Name: rs6059655
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.

rs6059655

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:34077942 (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: A=0.043953 (11634/264690, TOPMED)
A=0.045904 (6440/140294, GnomAD)
A=0.01536 (1209/78694, PAGE_STUDY) (+ 17 more)
A=0.05859 (2241/38248, ALFA)
A=0.00004 (1/28258, 14KJPN)
A=0.00006 (1/16760, 8.3KJPN)
A=0.0120 (77/6404, 1000G_30x)
A=0.0126 (63/5008, 1000G)
A=0.0277 (124/4480, Estonian)
A=0.1017 (392/3854, ALSPAC)
A=0.0912 (338/3708, TWINSUK)
A=0.0003 (1/2930, KOREAN)
A=0.0000 (0/1832, Korea1K)
A=0.094 (94/998, GoNL)
A=0.067 (40/600, NorthernSweden)
A=0.011 (6/556, SGDP_PRJ)
A=0.009 (2/216, Qatari)
A=0.000 (0/212, Vietnamese)
A=0.00 (0/56, Siberian)
A=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RALY : Intron Variant
Publications: 4 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	38248	A=0.05859	G=0.94141
European	Sub	25176	A=0.07213	G=0.92787
African	Sub	3478	A=0.0147	G=0.9853
African Others	Sub	124	A=0.000	G=1.000
African American	Sub	3354	A=0.0152	G=0.9848
Asian	Sub	184	A=0.000	G=1.000
East Asian	Sub	152	A=0.000	G=1.000
Other Asian	Sub	32	A=0.00	G=1.00
Latin American 1	Sub	244	A=0.037	G=0.963
Latin American 2	Sub	4784	A=0.0178	G=0.9822
South Asian	Sub	136	A=0.029	G=0.971
Other	Sub	4246	A=0.0650	G=0.9350

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=0.043953	G=0.956047
gnomAD - Genomes	Global	Study-wide	140294	A=0.045904	G=0.954096
gnomAD - Genomes	European	Sub	75970	A=0.06978	G=0.93022
gnomAD - Genomes	African	Sub	42050	A=0.01508	G=0.98492
gnomAD - Genomes	American	Sub	13666	A=0.02664	G=0.97336
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	A=0.0238	G=0.9762
gnomAD - Genomes	East Asian	Sub	3134	A=0.0000	G=1.0000
gnomAD - Genomes	Other	Sub	2152	A=0.0288	G=0.9712
The PAGE Study	Global	Study-wide	78694	A=0.01536	G=0.98464
The PAGE Study	AfricanAmerican	Sub	32508	A=0.01701	G=0.98299
The PAGE Study	Mexican	Sub	10810	A=0.01388	G=0.98612
The PAGE Study	Asian	Sub	8318	A=0.0004	G=0.9996
The PAGE Study	PuertoRican	Sub	7918	A=0.0165	G=0.9835
The PAGE Study	NativeHawaiian	Sub	4534	A=0.0232	G=0.9768
The PAGE Study	Cuban	Sub	4230	A=0.0215	G=0.9785
The PAGE Study	Dominican	Sub	3828	A=0.0125	G=0.9875
The PAGE Study	CentralAmerican	Sub	2450	A=0.0127	G=0.9873
The PAGE Study	SouthAmerican	Sub	1982	A=0.0161	G=0.9839
The PAGE Study	NativeAmerican	Sub	1260	A=0.0444	G=0.9556
The PAGE Study	SouthAsian	Sub	856	A=0.011	G=0.989
Allele Frequency Aggregator	Total	Global	38248	A=0.05859	G=0.94141
Allele Frequency Aggregator	European	Sub	25176	A=0.07213	G=0.92787
Allele Frequency Aggregator	Latin American 2	Sub	4784	A=0.0178	G=0.9822
Allele Frequency Aggregator	Other	Sub	4246	A=0.0650	G=0.9350
Allele Frequency Aggregator	African	Sub	3478	A=0.0147	G=0.9853
Allele Frequency Aggregator	Latin American 1	Sub	244	A=0.037	G=0.963
Allele Frequency Aggregator	Asian	Sub	184	A=0.000	G=1.000
Allele Frequency Aggregator	South Asian	Sub	136	A=0.029	G=0.971
14KJPN	JAPANESE	Study-wide	28258	A=0.00004	G=0.99996
8.3KJPN	JAPANESE	Study-wide	16760	A=0.00006	G=0.99994
1000Genomes_30x	Global	Study-wide	6404	A=0.0120	G=0.9880
1000Genomes_30x	African	Sub	1786	A=0.0034	G=0.9966
1000Genomes_30x	Europe	Sub	1266	A=0.0403	G=0.9597
1000Genomes_30x	South Asian	Sub	1202	A=0.0108	G=0.9892
1000Genomes_30x	East Asian	Sub	1170	A=0.0000	G=1.0000
1000Genomes_30x	American	Sub	980	A=0.007	G=0.993
1000Genomes	Global	Study-wide	5008	A=0.0126	G=0.9874
1000Genomes	African	Sub	1322	A=0.0030	G=0.9970
1000Genomes	East Asian	Sub	1008	A=0.0000	G=1.0000
1000Genomes	Europe	Sub	1006	A=0.0417	G=0.9583
1000Genomes	South Asian	Sub	978	A=0.012	G=0.988
1000Genomes	American	Sub	694	A=0.007	G=0.993
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.0277	G=0.9723
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.1017	G=0.8983
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.0912	G=0.9088
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.0003	G=0.9997
Korean Genome Project	KOREAN	Study-wide	1832	A=0.0000	G=1.0000
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.094	G=0.906
Northern Sweden	ACPOP	Study-wide	600	A=0.067	G=0.933
SGDP_PRJ	Global	Study-wide	556	A=0.011	G=0.989
Qatari	Global	Study-wide	216	A=0.009	G=0.991
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.000	G=1.000
Siberian	Global	Study-wide	56	A=0.00	G=1.00
The Danish reference pan genome	Danish	Study-wide	40	A=0.07	G=0.93

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 20	NC_000020.11:g.34077942A>G
GRCh37.p13 chr 20	NC_000020.10:g.32665748A>G

Gene: RALY, RALY heterogeneous nuclear ribonucleoprotein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RALY transcript variant 2	NM_007367.4:c.829-563A>G	N/A	Intron Variant
RALY transcript variant 1	NM_016732.3:c.877-563A>G	N/A	Intron Variant
RALY transcript variant X1	XM_005260334.6:c.877-563A… XM_005260334.6:c.877-563A>G	N/A	Intron Variant
RALY transcript variant X5	XM_005260336.6:c.829-563A… XM_005260336.6:c.829-563A>G	N/A	Intron Variant
RALY transcript variant X3	XM_011528695.4:c.877-563A… XM_011528695.4:c.877-563A>G	N/A	Intron Variant
RALY transcript variant X2	XM_017027731.3:c.877-563A… XM_017027731.3:c.877-563A>G	N/A	Intron Variant
RALY transcript variant X4	XM_047440015.1:c.877-563A… XM_047440015.1:c.877-563A>G	N/A	Intron Variant
RALY transcript variant X6	XM_047440016.1:c.829-563A… XM_047440016.1:c.829-563A>G	N/A	Intron 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 20	NC_000020.11:g.34077942=	NC_000020.11:g.34077942A>G
GRCh37.p13 chr 20	NC_000020.10:g.32665748=	NC_000020.10:g.32665748A>G
RALY transcript variant 2	NM_007367.3:c.829-563=	NM_007367.3:c.829-563A>G
RALY transcript variant 2	NM_007367.4:c.829-563=	NM_007367.4:c.829-563A>G
RALY transcript variant 1	NM_016732.2:c.877-563=	NM_016732.2:c.877-563A>G
RALY transcript variant 1	NM_016732.3:c.877-563=	NM_016732.3:c.877-563A>G
RALY transcript variant X1	XM_005260334.1:c.877-563=	XM_005260334.1:c.877-563A>G
RALY transcript variant X1	XM_005260334.6:c.877-563=	XM_005260334.6:c.877-563A>G
RALY transcript variant X2	XM_005260335.1:c.877-563=	XM_005260335.1:c.877-563A>G
RALY transcript variant X3	XM_005260336.1:c.829-563=	XM_005260336.1:c.829-563A>G
RALY transcript variant X5	XM_005260336.6:c.829-563=	XM_005260336.6:c.829-563A>G
RALY transcript variant X3	XM_011528695.4:c.877-563=	XM_011528695.4:c.877-563A>G
RALY transcript variant X2	XM_017027731.3:c.877-563=	XM_017027731.3:c.877-563A>G
RALY transcript variant X4	XM_047440015.1:c.877-563=	XM_047440015.1:c.877-563A>G
RALY transcript variant X6	XM_047440016.1:c.829-563=	XM_047440016.1:c.829-563A>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#.

103 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss8374512	Apr 21, 2003 (114)
2	BCM_SSAHASNP	ss10954674	Jul 11, 2003 (117)
3	WI_SSAHASNP	ss12482893	Jul 11, 2003 (117)
4	CSHL-HAPMAP	ss19473387	Feb 27, 2004 (120)
5	CSHL-HAPMAP	ss20122868	Feb 27, 2004 (120)
6	SSAHASNP	ss21772341	Apr 05, 2004 (121)
7	HGSV	ss78522459	Dec 06, 2007 (129)
8	HGSV	ss80757479	Dec 15, 2007 (130)
9	HGSV	ss83658565	Dec 15, 2007 (130)
10	HGSV	ss85667798	Dec 15, 2007 (130)
11	BCMHGSC_JDW	ss91687645	Mar 24, 2008 (129)
12	HUMANGENOME_JCVI	ss96193844	Feb 04, 2009 (130)
13	BGI	ss106186640	Feb 04, 2009 (130)
14	1000GENOMES	ss111929712	Jan 25, 2009 (130)
15	1000GENOMES	ss113283370	Jan 25, 2009 (130)
16	IGMI-SNU	ss115473102	Feb 04, 2009 (130)
17	ILLUMINA-UK	ss117532141	Feb 14, 2009 (130)
18	ENSEMBL	ss135724542	Dec 01, 2009 (131)
19	ENSEMBL	ss138237551	Dec 01, 2009 (131)
20	GMI	ss156384955	Dec 01, 2009 (131)
21	ILLUMINA	ss161066889	Dec 01, 2009 (131)
22	COMPLETE_GENOMICS	ss168073112	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss169497707	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss172049635	Jul 04, 2010 (132)
25	BUSHMAN	ss203876988	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss208647318	Jul 04, 2010 (132)
27	1000GENOMES	ss228333546	Jul 14, 2010 (132)
28	1000GENOMES	ss237818852	Jul 15, 2010 (132)
29	1000GENOMES	ss243992501	Jul 15, 2010 (132)
30	BL	ss255611880	May 09, 2011 (134)
31	GMI	ss283367676	May 04, 2012 (137)
32	GMI	ss287452553	Apr 25, 2013 (138)
33	PJP	ss292644451	May 09, 2011 (134)
34	ILLUMINA	ss479182201	Sep 08, 2015 (146)
35	ILLUMINA	ss479898672	May 04, 2012 (137)
36	ILLUMINA	ss484180857	May 04, 2012 (137)
37	ILLUMINA	ss533374992	Sep 08, 2015 (146)
38	TISHKOFF	ss566224107	Apr 25, 2013 (138)
39	SSMP	ss662106482	Apr 25, 2013 (138)
40	ILLUMINA	ss779672691	Sep 08, 2015 (146)
41	ILLUMINA	ss781096311	Sep 08, 2015 (146)
42	ILLUMINA	ss835146215	Sep 08, 2015 (146)
43	EVA-GONL	ss994683011	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1082177772	Aug 21, 2014 (142)
45	1000GENOMES	ss1364621839	Aug 21, 2014 (142)
46	DDI	ss1429044844	Apr 01, 2015 (144)
47	EVA_GENOME_DK	ss1579493372	Apr 01, 2015 (144)
48	EVA_UK10K_ALSPAC	ss1638700497	Apr 01, 2015 (144)
49	EVA_UK10K_TWINSUK	ss1681694530	Apr 01, 2015 (144)
50	EVA_DECODE	ss1698741627	Apr 01, 2015 (144)
51	HAMMER_LAB	ss1809485793	Sep 08, 2015 (146)
52	WEILL_CORNELL_DGM	ss1938196529	Feb 12, 2016 (147)
53	ILLUMINA	ss1959911422	Feb 12, 2016 (147)
54	GENOMED	ss1969126225	Jul 19, 2016 (147)
55	JJLAB	ss2029880638	Sep 14, 2016 (149)
56	USC_VALOUEV	ss2158444675	Dec 20, 2016 (150)
57	HUMAN_LONGEVITY	ss2242437358	Dec 20, 2016 (150)
58	SYSTEMSBIOZJU	ss2629434114	Nov 08, 2017 (151)
59	ILLUMINA	ss2633793383	Nov 08, 2017 (151)
60	GRF	ss2704134530	Nov 08, 2017 (151)
61	GNOMAD	ss2966988896	Nov 08, 2017 (151)
62	SWEGEN	ss3018125161	Nov 08, 2017 (151)
63	ILLUMINA	ss3022115025	Nov 08, 2017 (151)
64	BIOINF_KMB_FNS_UNIBA	ss3028773352	Nov 08, 2017 (151)
65	CSHL	ss3352496591	Nov 08, 2017 (151)
66	ILLUMINA	ss3628382230	Oct 12, 2018 (152)
67	ILLUMINA	ss3631750223	Oct 12, 2018 (152)
68	ILLUMINA	ss3636525708	Oct 12, 2018 (152)
69	ILLUMINA	ss3642179793	Oct 12, 2018 (152)
70	URBANLAB	ss3651014163	Oct 12, 2018 (152)
71	ILLUMINA	ss3652570036	Oct 12, 2018 (152)
72	EGCUT_WGS	ss3684804849	Jul 13, 2019 (153)
73	EVA_DECODE	ss3706872624	Jul 13, 2019 (153)
74	ILLUMINA	ss3725911622	Jul 13, 2019 (153)
75	ACPOP	ss3743364044	Jul 13, 2019 (153)
76	EVA	ss3758596361	Jul 13, 2019 (153)
77	PAGE_CC	ss3772045063	Jul 13, 2019 (153)
78	PACBIO	ss3788638700	Jul 13, 2019 (153)
79	PACBIO	ss3793532566	Jul 13, 2019 (153)
80	PACBIO	ss3798419462	Jul 13, 2019 (153)
81	KHV_HUMAN_GENOMES	ss3821765457	Jul 13, 2019 (153)
82	EVA	ss3835655719	Apr 27, 2020 (154)
83	EVA	ss3841454286	Apr 27, 2020 (154)
84	EVA	ss3846966727	Apr 27, 2020 (154)
85	SGDP_PRJ	ss3889026667	Apr 27, 2020 (154)
86	KRGDB	ss3939297192	Apr 27, 2020 (154)
87	KOGIC	ss3982203714	Apr 27, 2020 (154)
88	TOPMED	ss5087281919	Apr 26, 2021 (155)
89	TOMMO_GENOMICS	ss5229471373	Apr 26, 2021 (155)
90	1000G_HIGH_COVERAGE	ss5308667727	Oct 13, 2022 (156)
91	EVA	ss5316004785	Oct 13, 2022 (156)
92	HUGCELL_USP	ss5500957873	Oct 13, 2022 (156)
93	EVA	ss5512205540	Oct 13, 2022 (156)
94	1000G_HIGH_COVERAGE	ss5615063904	Oct 13, 2022 (156)
95	SANFORD_IMAGENETICS	ss5624484427	Oct 13, 2022 (156)
96	SANFORD_IMAGENETICS	ss5663144428	Oct 13, 2022 (156)
97	TOMMO_GENOMICS	ss5789215135	Oct 13, 2022 (156)
98	YY_MCH	ss5818015313	Oct 13, 2022 (156)
99	EVA	ss5845644459	Oct 13, 2022 (156)
100	EVA	ss5853126648	Oct 13, 2022 (156)
101	EVA	ss5923275127	Oct 13, 2022 (156)
102	EVA	ss5958053641	Oct 13, 2022 (156)
103	EVA	ss5979614728	Oct 13, 2022 (156)
104	1000Genomes	NC_000020.10 - 32665748	Oct 12, 2018 (152)
105	1000Genomes_30x	NC_000020.11 - 34077942	Oct 13, 2022 (156)
106	The Avon Longitudinal Study of Parents and Children	NC_000020.10 - 32665748	Oct 12, 2018 (152)
107	Genetic variation in the Estonian population	NC_000020.10 - 32665748	Oct 12, 2018 (152)
108	The Danish reference pan genome	NC_000020.10 - 32665748	Apr 27, 2020 (154)
109	gnomAD - Genomes	NC_000020.11 - 34077942	Apr 26, 2021 (155)
110	Genome of the Netherlands Release 5	NC_000020.10 - 32665748	Apr 27, 2020 (154)
111	KOREAN population from KRGDB	NC_000020.10 - 32665748	Apr 27, 2020 (154)
112	Korean Genome Project	NC_000020.11 - 34077942	Apr 27, 2020 (154)
113	Northern Sweden	NC_000020.10 - 32665748	Jul 13, 2019 (153)
114	The PAGE Study	NC_000020.11 - 34077942	Jul 13, 2019 (153)
115	Qatari	NC_000020.10 - 32665748	Apr 27, 2020 (154)
116	SGDP_PRJ	NC_000020.10 - 32665748	Apr 27, 2020 (154)
117	Siberian	NC_000020.10 - 32665748	Apr 27, 2020 (154)
118	8.3KJPN	NC_000020.10 - 32665748	Apr 26, 2021 (155)
119	14KJPN	NC_000020.11 - 34077942	Oct 13, 2022 (156)
120	TopMed	NC_000020.11 - 34077942	Apr 26, 2021 (155)
121	UK 10K study - Twins	NC_000020.10 - 32665748	Oct 12, 2018 (152)
122	A Vietnamese Genetic Variation Database	NC_000020.10 - 32665748	Jul 13, 2019 (153)
123	ALFA	NC_000020.11 - 34077942	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)
rs6579136	Aug 26, 2003 (117)
rs58278223	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss78522459, ss80757479, ss83658565, ss85667798, ss91687645, ss111929712, ss113283370, ss117532141, ss168073112, ss169497707, ss172049635, ss203876988, ss208647318, ss255611880, ss283367676, ss287452553, ss292644451, ss484180857, ss1698741627	NC_000020.9:32129408:A:G	NC_000020.11:34077941:A:G	(self)
78079916, 43220252, 30543097, 5658311, 19257427, 46474586, 16648909, 20238451, 41043647, 10961029, 87440680, 43220252, 9539743, ss228333546, ss237818852, ss243992501, ss479182201, ss479898672, ss533374992, ss566224107, ss662106482, ss779672691, ss781096311, ss835146215, ss994683011, ss1082177772, ss1364621839, ss1429044844, ss1579493372, ss1638700497, ss1681694530, ss1809485793, ss1938196529, ss1959911422, ss1969126225, ss2029880638, ss2158444675, ss2629434114, ss2633793383, ss2704134530, ss2966988896, ss3018125161, ss3022115025, ss3352496591, ss3628382230, ss3631750223, ss3636525708, ss3642179793, ss3652570036, ss3684804849, ss3743364044, ss3758596361, ss3788638700, ss3793532566, ss3798419462, ss3835655719, ss3841454286, ss3889026667, ss3939297192, ss5229471373, ss5316004785, ss5512205540, ss5624484427, ss5663144428, ss5845644459, ss5958053641, ss5979614728	NC_000020.10:32665747:A:G	NC_000020.11:34077941:A:G	(self)
102589839, 550750427, 38581715, 1266532, 123052239, 362390864, 13796037748, ss2242437358, ss3028773352, ss3651014163, ss3706872624, ss3725911622, ss3772045063, ss3821765457, ss3846966727, ss3982203714, ss5087281919, ss5308667727, ss5500957873, ss5615063904, ss5789215135, ss5818015313, ss5853126648, ss5923275127	NC_000020.11:34077941:A:G	NC_000020.11:34077941:A:G	(self)
ss96193844, ss106186640, ss115473102, ss135724542, ss138237551, ss156384955, ss161066889	NT_011362.10:2861839:A:G	NC_000020.11:34077941:A:G	(self)
ss8374512, ss10954674, ss12482893, ss19473387, ss20122868, ss21772341	NT_028392.4:2832515:A:G	NC_000020.11:34077941:A:G	(self)

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

4 citations for rs6059655

PMID	Title	Author	Year	Journal
25077817	Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.	Barrett JH et al.	2015	International journal of cancer
25705849	A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots.	Jacobs LC et al.	2015	The Journal of investigative dermatology
27424798	Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma.	Chahal HS et al.	2016	Nature communications
27539887	Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.	Chahal HS et al.	2016	Nature communications

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
Top▲ Help
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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs6059655