Name: rs17128291
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs17128291

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:92416482 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: A>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.109891 (29087/264690, TOPMED)
G=0.111968 (15693/140156, GnomAD)
G=0.14166 (13345/94206, ALFA) (+ 23 more)
G=0.07049 (5547/78696, PAGE_STUDY)
G=0.07485 (2115/28258, 14KJPN)
G=0.07422 (1244/16760, 8.3KJPN)
G=0.0817 (523/6404, 1000G_30x)
G=0.0851 (426/5008, 1000G)
G=0.1489 (667/4480, Estonian)
G=0.1575 (607/3854, ALSPAC)
G=0.1437 (533/3708, TWINSUK)
G=0.0811 (237/2922, KOREAN)
G=0.0777 (162/2084, HGDP_Stanford)
G=0.0895 (164/1832, Korea1K)
G=0.0840 (150/1786, HapMap)
G=0.0741 (84/1134, Daghestan)
G=0.156 (156/998, GoNL)
G=0.097 (61/626, Chileans)
G=0.150 (90/600, NorthernSweden)
G=0.167 (36/216, Qatari)
G=0.047 (10/212, Vietnamese)
G=0.45 (36/80, Ancient Sardinia)
A=0.47 (36/76, SGDP_PRJ)
G=0.10 (4/40, GENOME_DK)
A=0.50 (6/12, Siberian)
G=0.50 (6/12, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC24A4 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	94206	A=0.85834	G=0.14166
European	Sub	77536	A=0.84148	G=0.15852
African	Sub	5426	A=0.9692	G=0.0308
African Others	Sub	182	A=1.000	G=0.000
African American	Sub	5244	A=0.9682	G=0.0318
Asian	Sub	312	A=0.920	G=0.080
East Asian	Sub	240	A=0.912	G=0.087
Other Asian	Sub	72	A=0.94	G=0.06
Latin American 1	Sub	392	A=0.857	G=0.143
Latin American 2	Sub	3386	A=0.9176	G=0.0824
South Asian	Sub	4974	A=0.9371	G=0.0629
Other	Sub	2180	A=0.9018	G=0.0982

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	A=0.890109	G=0.109891
gnomAD - Genomes	Global	Study-wide	140156	A=0.888032	G=0.111968
gnomAD - Genomes	European	Sub	75896	A=0.84612	G=0.15388
gnomAD - Genomes	African	Sub	42022	A=0.97016	G=0.02984
gnomAD - Genomes	American	Sub	13634	A=0.88008	G=0.11992
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.8374	G=0.1626
gnomAD - Genomes	East Asian	Sub	3130	A=0.8958	G=0.1042
gnomAD - Genomes	Other	Sub	2152	A=0.8796	G=0.1204
Allele Frequency Aggregator	Total	Global	94206	A=0.85834	G=0.14166
Allele Frequency Aggregator	European	Sub	77536	A=0.84148	G=0.15852
Allele Frequency Aggregator	African	Sub	5426	A=0.9692	G=0.0308
Allele Frequency Aggregator	South Asian	Sub	4974	A=0.9371	G=0.0629
Allele Frequency Aggregator	Latin American 2	Sub	3386	A=0.9176	G=0.0824
Allele Frequency Aggregator	Other	Sub	2180	A=0.9018	G=0.0982
Allele Frequency Aggregator	Latin American 1	Sub	392	A=0.857	G=0.143
Allele Frequency Aggregator	Asian	Sub	312	A=0.920	G=0.080
The PAGE Study	Global	Study-wide	78696	A=0.92951	G=0.07049
The PAGE Study	AfricanAmerican	Sub	32514	A=0.96617	G=0.03383
The PAGE Study	Mexican	Sub	10810	A=0.91961	G=0.08039
The PAGE Study	Asian	Sub	8316	A=0.9241	G=0.0759
The PAGE Study	PuertoRican	Sub	7916	A=0.8497	G=0.1503
The PAGE Study	NativeHawaiian	Sub	4534	A=0.9347	G=0.0653
The PAGE Study	Cuban	Sub	4230	A=0.8582	G=0.1418
The PAGE Study	Dominican	Sub	3828	A=0.9117	G=0.0883
The PAGE Study	CentralAmerican	Sub	2450	A=0.9273	G=0.0727
The PAGE Study	SouthAmerican	Sub	1982	A=0.9137	G=0.0863
The PAGE Study	NativeAmerican	Sub	1260	A=0.8984	G=0.1016
The PAGE Study	SouthAsian	Sub	856	A=0.946	G=0.054
14KJPN	JAPANESE	Study-wide	28258	A=0.92515	G=0.07485
8.3KJPN	JAPANESE	Study-wide	16760	A=0.92578	G=0.07422
1000Genomes_30x	Global	Study-wide	6404	A=0.9183	G=0.0817
1000Genomes_30x	African	Sub	1786	A=0.9905	G=0.0095
1000Genomes_30x	Europe	Sub	1266	A=0.8412	G=0.1588
1000Genomes_30x	South Asian	Sub	1202	A=0.9176	G=0.0824
1000Genomes_30x	East Asian	Sub	1170	A=0.9085	G=0.0915
1000Genomes_30x	American	Sub	980	A=0.899	G=0.101
1000Genomes	Global	Study-wide	5008	A=0.9149	G=0.0851
1000Genomes	African	Sub	1322	A=0.9909	G=0.0091
1000Genomes	East Asian	Sub	1008	A=0.9097	G=0.0903
1000Genomes	Europe	Sub	1006	A=0.8419	G=0.1581
1000Genomes	South Asian	Sub	978	A=0.910	G=0.090
1000Genomes	American	Sub	694	A=0.890	G=0.110
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.8511	G=0.1489
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.8425	G=0.1575
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.8563	G=0.1437
KOREAN population from KRGDB	KOREAN	Study-wide	2922	A=0.9189	G=0.0811
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.9223	G=0.0777
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.936	G=0.064
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.913	G=0.087
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.891	G=0.109
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.831	G=0.169
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.996	G=0.004
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.995	G=0.005
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.97	G=0.03
Korean Genome Project	KOREAN	Study-wide	1832	A=0.9105	G=0.0895
HapMap	Global	Study-wide	1786	A=0.9160	G=0.0840
HapMap	American	Sub	770	A=0.897	G=0.103
HapMap	African	Sub	586	A=0.976	G=0.024
HapMap	Asian	Sub	254	A=0.898	G=0.102
HapMap	Europe	Sub	176	A=0.824	G=0.176
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	A=0.9259	G=0.0741
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	A=0.949	G=0.051
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	A=0.903	G=0.097
Genome-wide autozygosity in Daghestan	Central Asia	Sub	120	A=0.892	G=0.108
Genome-wide autozygosity in Daghestan	Europe	Sub	108	A=0.843	G=0.157
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	A=0.95	G=0.05
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	A=0.92	G=0.08
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.844	G=0.156
Chileans	Chilean	Study-wide	626	A=0.903	G=0.097
Northern Sweden	ACPOP	Study-wide	600	A=0.850	G=0.150
Qatari	Global	Study-wide	216	A=0.833	G=0.167
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.953	G=0.047
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	80	A=0.55	G=0.45
SGDP_PRJ	Global	Study-wide	76	A=0.47	G=0.53
The Danish reference pan genome	Danish	Study-wide	40	A=0.90	G=0.10
Siberian	Global	Study-wide	12	A=0.50	G=0.50

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 14	NC_000014.9:g.92416482A>G
GRCh37.p13 chr 14	NC_000014.8:g.92882826A>G
SLC24A4 RefSeqGene	NG_023408.1:g.98902A>G

Gene: SLC24A4, solute carrier family 24 member 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC24A4 transcript variant 4	NM_001378620.1:c.242-1743… NM_001378620.1:c.242-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant 1	NM_153646.4:c.242-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant 2	NM_153647.4:c.242-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant 3	NM_153648.4:c.50-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant X5	XM_005267342.2:c.-87+8048… XM_005267342.2:c.-87+8048A>G	N/A	Intron Variant
SLC24A4 transcript variant X1	XM_011536436.3:c.383-1743… XM_011536436.3:c.383-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant X2	XM_011536437.3:c.383-1743… XM_011536437.3:c.383-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant X3	XM_024449478.2:c.242-1743… XM_024449478.2:c.242-17430A>G	N/A	Intron Variant
SLC24A4 transcript variant X4	XM_011536440.2:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	A=	G
GRCh38.p14 chr 14	NC_000014.9:g.92416482=	NC_000014.9:g.92416482A>G
GRCh37.p13 chr 14	NC_000014.8:g.92882826=	NC_000014.8:g.92882826A>G
SLC24A4 RefSeqGene	NG_023408.1:g.98902=	NG_023408.1:g.98902A>G
SLC24A4 transcript variant 4	NM_001378620.1:c.242-17430=	NM_001378620.1:c.242-17430A>G
SLC24A4 transcript variant 1	NM_153646.3:c.242-17430=	NM_153646.3:c.242-17430A>G
SLC24A4 transcript variant 1	NM_153646.4:c.242-17430=	NM_153646.4:c.242-17430A>G
SLC24A4 transcript variant 2	NM_153647.3:c.242-17430=	NM_153647.3:c.242-17430A>G
SLC24A4 transcript variant 2	NM_153647.4:c.242-17430=	NM_153647.4:c.242-17430A>G
SLC24A4 transcript variant 3	NM_153648.3:c.50-17430=	NM_153648.3:c.50-17430A>G
SLC24A4 transcript variant 3	NM_153648.4:c.50-17430=	NM_153648.4:c.50-17430A>G
SLC24A4 transcript variant X1	XM_005267341.1:c.242-17430=	XM_005267341.1:c.242-17430A>G
SLC24A4 transcript variant X6	XM_005267342.1:c.-87+8048=	XM_005267342.1:c.-87+8048A>G
SLC24A4 transcript variant X5	XM_005267342.2:c.-87+8048=	XM_005267342.2:c.-87+8048A>G
SLC24A4 transcript variant X1	XM_011536436.3:c.383-17430=	XM_011536436.3:c.383-17430A>G
SLC24A4 transcript variant X2	XM_011536437.3:c.383-17430=	XM_011536437.3:c.383-17430A>G
SLC24A4 transcript variant X3	XM_024449478.2:c.242-17430=	XM_024449478.2:c.242-17430A>G

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

88 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss24134210	Sep 20, 2004 (123)
2	AFFY	ss66166263	Dec 01, 2006 (127)
3	ILLUMINA	ss66802668	Dec 01, 2006 (127)
4	ILLUMINA	ss67178152	Dec 01, 2006 (127)
5	ILLUMINA	ss67540912	Dec 01, 2006 (127)
6	PERLEGEN	ss69166388	May 17, 2007 (127)
7	ILLUMINA	ss70450797	May 17, 2007 (127)
8	ILLUMINA	ss70656175	May 25, 2008 (130)
9	ILLUMINA	ss71216035	May 17, 2007 (127)
10	ILLUMINA	ss75841129	Dec 07, 2007 (129)
11	AFFY	ss76214854	Dec 08, 2007 (130)
12	KRIBB_YJKIM	ss85367368	Dec 15, 2007 (130)
13	BGI	ss106407460	Feb 05, 2009 (130)
14	1000GENOMES	ss108564183	Jan 23, 2009 (130)
15	ILLUMINA	ss121787369	Dec 01, 2009 (131)
16	ILLUMINA	ss153634078	Dec 01, 2009 (131)
17	ILLUMINA	ss159309844	Dec 01, 2009 (131)
18	ILLUMINA	ss170752565	Jul 04, 2010 (132)
19	ILLUMINA	ss172758132	Jul 04, 2010 (132)
20	AFFY	ss172839736	Jul 04, 2010 (132)
21	1000GENOMES	ss236654432	Jul 15, 2010 (132)
22	1000GENOMES	ss243066003	Jul 15, 2010 (132)
23	GMI	ss282113397	May 04, 2012 (137)
24	GMI	ss286892645	Apr 25, 2013 (138)
25	ILLUMINA	ss535888807	Sep 08, 2015 (146)
26	SSMP	ss659968471	Apr 25, 2013 (138)
27	ILLUMINA	ss825419530	Apr 01, 2015 (144)
28	ILLUMINA	ss832821906	Aug 21, 2014 (142)
29	ILLUMINA	ss833412736	Aug 21, 2014 (142)
30	EVA-GONL	ss991449712	Aug 21, 2014 (142)
31	JMKIDD_LAB	ss1079883648	Aug 21, 2014 (142)
32	1000GENOMES	ss1352149717	Aug 21, 2014 (142)
33	HAMMER_LAB	ss1397688779	Sep 08, 2015 (146)
34	DDI	ss1427510911	Apr 01, 2015 (144)
35	EVA_GENOME_DK	ss1577431964	Apr 01, 2015 (144)
36	EVA_UK10K_ALSPAC	ss1632352913	Apr 01, 2015 (144)
37	EVA_UK10K_TWINSUK	ss1675346946	Apr 01, 2015 (144)
38	EVA_DECODE	ss1695463649	Apr 01, 2015 (144)
39	EVA_SVP	ss1713466557	Apr 01, 2015 (144)
40	WEILL_CORNELL_DGM	ss1934819763	Feb 12, 2016 (147)
41	ILLUMINA	ss1959577233	Feb 12, 2016 (147)
42	JJLAB	ss2028193957	Sep 14, 2016 (149)
43	USC_VALOUEV	ss2156576991	Dec 20, 2016 (150)
44	HUMAN_LONGEVITY	ss2204359163	Dec 20, 2016 (150)
45	SYSTEMSBIOZJU	ss2628586359	Nov 08, 2017 (151)
46	GRF	ss2701012797	Nov 08, 2017 (151)
47	ILLUMINA	ss2710808051	Nov 08, 2017 (151)
48	GNOMAD	ss2930942770	Nov 08, 2017 (151)
49	SWEGEN	ss3012669316	Nov 08, 2017 (151)
50	ILLUMINA	ss3021594770	Nov 08, 2017 (151)
51	BIOINF_KMB_FNS_UNIBA	ss3027924113	Nov 08, 2017 (151)
52	CSHL	ss3350940616	Nov 08, 2017 (151)
53	ILLUMINA	ss3627286514	Oct 12, 2018 (152)
54	ILLUMINA	ss3638066928	Oct 12, 2018 (152)
55	ILLUMINA	ss3639047143	Oct 12, 2018 (152)
56	ILLUMINA	ss3639528539	Oct 12, 2018 (152)
57	ILLUMINA	ss3643052473	Oct 12, 2018 (152)
58	ILLUMINA	ss3651992586	Oct 12, 2018 (152)
59	EGCUT_WGS	ss3679934142	Jul 13, 2019 (153)
60	EVA_DECODE	ss3697249980	Jul 13, 2019 (153)
61	ILLUMINA	ss3725471470	Jul 13, 2019 (153)
62	ACPOP	ss3740637779	Jul 13, 2019 (153)
63	EVA	ss3752678372	Jul 13, 2019 (153)
64	PAGE_CC	ss3771807993	Jul 13, 2019 (153)
65	PACBIO	ss3787747118	Jul 13, 2019 (153)
66	PACBIO	ss3792772832	Jul 13, 2019 (153)
67	PACBIO	ss3797657359	Jul 13, 2019 (153)
68	KHV_HUMAN_GENOMES	ss3818005451	Jul 13, 2019 (153)
69	EVA	ss3834068075	Apr 27, 2020 (154)
70	HGDP	ss3847513270	Apr 27, 2020 (154)
71	SGDP_PRJ	ss3882109171	Apr 27, 2020 (154)
72	KRGDB	ss3931189485	Apr 27, 2020 (154)
73	KOGIC	ss3975500580	Apr 27, 2020 (154)
74	EVA	ss3985697552	Apr 26, 2021 (155)
75	EVA	ss4017685443	Apr 26, 2021 (155)
76	TOPMED	ss4980511582	Apr 26, 2021 (155)
77	TOMMO_GENOMICS	ss5214530628	Apr 26, 2021 (155)
78	1000G_HIGH_COVERAGE	ss5297229685	Oct 16, 2022 (156)
79	EVA	ss5417094842	Oct 16, 2022 (156)
80	HUGCELL_USP	ss5491179790	Oct 16, 2022 (156)
81	EVA	ss5511344219	Oct 16, 2022 (156)
82	1000G_HIGH_COVERAGE	ss5598018061	Oct 16, 2022 (156)
83	SANFORD_IMAGENETICS	ss5656791600	Oct 16, 2022 (156)
84	TOMMO_GENOMICS	ss5767706932	Oct 16, 2022 (156)
85	YY_MCH	ss5815002350	Oct 16, 2022 (156)
86	EVA	ss5841508106	Oct 16, 2022 (156)
87	EVA	ss5902500046	Oct 16, 2022 (156)
88	EVA	ss5948254242	Oct 16, 2022 (156)
89	1000Genomes	NC_000014.8 - 92882826	Oct 12, 2018 (152)
90	1000Genomes_30x	NC_000014.9 - 92416482	Oct 16, 2022 (156)
91	The Avon Longitudinal Study of Parents and Children	NC_000014.8 - 92882826	Oct 12, 2018 (152)
92	Chileans	NC_000014.8 - 92882826	Apr 27, 2020 (154)
93	Genome-wide autozygosity in Daghestan	NC_000014.7 - 91952579	Apr 27, 2020 (154)
94	Genetic variation in the Estonian population	NC_000014.8 - 92882826	Oct 12, 2018 (152)
95	The Danish reference pan genome	NC_000014.8 - 92882826	Apr 27, 2020 (154)
96	gnomAD - Genomes	NC_000014.9 - 92416482	Apr 26, 2021 (155)
97	Genome of the Netherlands Release 5	NC_000014.8 - 92882826	Apr 27, 2020 (154)
98	HGDP-CEPH-db Supplement 1	NC_000014.7 - 91952579	Apr 27, 2020 (154)
99	HapMap	NC_000014.9 - 92416482	Apr 27, 2020 (154)
100	KOREAN population from KRGDB	NC_000014.8 - 92882826	Apr 27, 2020 (154)
101	Korean Genome Project	NC_000014.9 - 92416482	Apr 27, 2020 (154)
102	Northern Sweden	NC_000014.8 - 92882826	Jul 13, 2019 (153)
103	The PAGE Study	NC_000014.9 - 92416482	Jul 13, 2019 (153)
104	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000014.8 - 92882826	Apr 26, 2021 (155)
105	Qatari	NC_000014.8 - 92882826	Apr 27, 2020 (154)
106	SGDP_PRJ	NC_000014.8 - 92882826	Apr 27, 2020 (154)
107	Siberian	NC_000014.8 - 92882826	Apr 27, 2020 (154)
108	8.3KJPN	NC_000014.8 - 92882826	Apr 26, 2021 (155)
109	14KJPN	NC_000014.9 - 92416482	Oct 16, 2022 (156)
110	TopMed	NC_000014.9 - 92416482	Apr 26, 2021 (155)
111	UK 10K study - Twins	NC_000014.8 - 92882826	Oct 12, 2018 (152)
112	A Vietnamese Genetic Variation Database	NC_000014.8 - 92882826	Jul 13, 2019 (153)
113	ALFA	NC_000014.9 - 92416482	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs56555445	May 25, 2008 (130)
rs59895870	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
159047, 191162, ss66166263, ss76214854, ss108564183, ss172839736, ss282113397, ss286892645, ss825419530, ss1397688779, ss1695463649, ss1713466557, ss3639047143, ss3639528539, ss3643052473, ss3847513270	NC_000014.7:91952578:A:G	NC_000014.9:92416481:A:G	(self)
65174127, 36224743, 145308, 25672390, 3723741, 16172473, 38366879, 13922644, 923479, 16861693, 34126151, 9093345, 72499935, 36224743, 8058596, ss236654432, ss243066003, ss535888807, ss659968471, ss832821906, ss833412736, ss991449712, ss1079883648, ss1352149717, ss1427510911, ss1577431964, ss1632352913, ss1675346946, ss1934819763, ss1959577233, ss2028193957, ss2156576991, ss2628586359, ss2701012797, ss2710808051, ss2930942770, ss3012669316, ss3021594770, ss3350940616, ss3627286514, ss3638066928, ss3651992586, ss3679934142, ss3740637779, ss3752678372, ss3787747118, ss3792772832, ss3797657359, ss3834068075, ss3882109171, ss3931189485, ss3985697552, ss4017685443, ss5214530628, ss5417094842, ss5511344219, ss5656791600, ss5841508106, ss5948254242	NC_000014.8:92882825:A:G	NC_000014.9:92416481:A:G	(self)
85543996, 459463328, 1203230, 31878581, 1029462, 101544036, 196057241, 8469066340, ss2204359163, ss3027924113, ss3697249980, ss3725471470, ss3771807993, ss3818005451, ss3975500580, ss4980511582, ss5297229685, ss5491179790, ss5598018061, ss5767706932, ss5815002350, ss5902500046	NC_000014.9:92416481:A:G	NC_000014.9:92416481:A:G	(self)
ss24134210, ss66802668, ss67178152, ss67540912, ss69166388, ss70450797, ss70656175, ss71216035, ss75841129, ss85367368, ss106407460, ss121787369, ss153634078, ss159309844, ss170752565, ss172758132	NT_026437.12:73882825:A:G	NC_000014.9:92416481:A:G	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs17128291

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs17128291