Name: rs7655217
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.

rs7655217

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:86310615 (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: C>A / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.400918 (106119/264690, TOPMED)
C=0.342431 (68389/199716, ALFA)
C=0.387888 (54250/139860, GnomAD) (+ 19 more)
C=0.41171 (11634/28258, 14KJPN)
C=0.41211 (6907/16760, 8.3KJPN)
C=0.4094 (2622/6404, 1000G_30x)
C=0.4060 (2033/5008, 1000G)
C=0.2998 (1343/4480, Estonian)
C=0.3134 (1208/3854, ALSPAC)
C=0.3255 (1207/3708, TWINSUK)
C=0.4990 (1462/2930, KOREAN)
C=0.3780 (787/2082, HGDP_Stanford)
C=0.4116 (778/1890, HapMap)
C=0.4973 (911/1832, Korea1K)
C=0.317 (316/998, GoNL)
C=0.350 (210/600, NorthernSweden)
C=0.260 (125/480, SGDP_PRJ)
C=0.394 (85/216, Qatari)
A=0.495 (104/210, Vietnamese)
C=0.30 (15/50, Siberian)
C=0.35 (14/40, GENOME_DK)
C=0.22 (8/36, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAPK10 : 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	199716	C=0.342431	A=0.657569
European	Sub	172618	C=0.337085	A=0.662915
African	Sub	7094	C=0.5120	A=0.4880
African Others	Sub	264	C=0.538	A=0.462
African American	Sub	6830	C=0.5110	A=0.4890
Asian	Sub	700	C=0.453	A=0.547
East Asian	Sub	554	C=0.439	A=0.561
Other Asian	Sub	146	C=0.507	A=0.493
Latin American 1	Sub	844	C=0.411	A=0.589
Latin American 2	Sub	6782	C=0.3477	A=0.6523
South Asian	Sub	5038	C=0.2616	A=0.7384
Other	Sub	6640	C=0.3358	A=0.6642

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	C=0.400918	A=0.599082
Allele Frequency Aggregator	Total	Global	199716	C=0.342431	A=0.657569
Allele Frequency Aggregator	European	Sub	172618	C=0.337085	A=0.662915
Allele Frequency Aggregator	African	Sub	7094	C=0.5120	A=0.4880
Allele Frequency Aggregator	Latin American 2	Sub	6782	C=0.3477	A=0.6523
Allele Frequency Aggregator	Other	Sub	6640	C=0.3358	A=0.6642
Allele Frequency Aggregator	South Asian	Sub	5038	C=0.2616	A=0.7384
Allele Frequency Aggregator	Latin American 1	Sub	844	C=0.411	A=0.589
Allele Frequency Aggregator	Asian	Sub	700	C=0.453	A=0.547
gnomAD - Genomes	Global	Study-wide	139860	C=0.387888	A=0.612112
gnomAD - Genomes	European	Sub	75776	C=0.32345	A=0.67655
gnomAD - Genomes	African	Sub	41870	C=0.50719	A=0.49281
gnomAD - Genomes	American	Sub	13620	C=0.37577	A=0.62423
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	C=0.2863	A=0.7137
gnomAD - Genomes	East Asian	Sub	3120	C=0.4942	A=0.5058
gnomAD - Genomes	Other	Sub	2152	C=0.4150	A=0.5850
14KJPN	JAPANESE	Study-wide	28258	C=0.41171	A=0.58829
8.3KJPN	JAPANESE	Study-wide	16760	C=0.41211	A=0.58789
1000Genomes_30x	Global	Study-wide	6404	C=0.4094	A=0.5906
1000Genomes_30x	African	Sub	1786	C=0.5414	A=0.4586
1000Genomes_30x	Europe	Sub	1266	C=0.3444	A=0.6556
1000Genomes_30x	South Asian	Sub	1202	C=0.2521	A=0.7479
1000Genomes_30x	East Asian	Sub	1170	C=0.4607	A=0.5393
1000Genomes_30x	American	Sub	980	C=0.385	A=0.615
1000Genomes	Global	Study-wide	5008	C=0.4060	A=0.5940
1000Genomes	African	Sub	1322	C=0.5280	A=0.4720
1000Genomes	East Asian	Sub	1008	C=0.4613	A=0.5387
1000Genomes	Europe	Sub	1006	C=0.3539	A=0.6461
1000Genomes	South Asian	Sub	978	C=0.248	A=0.752
1000Genomes	American	Sub	694	C=0.390	A=0.610
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.2998	A=0.7002
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.3134	A=0.6866
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.3255	A=0.6745
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.4990	A=0.5010, T=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	C=0.3780	A=0.6220
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	468	C=0.474	A=0.526
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.302	A=0.698
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.357	A=0.643
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.388	A=0.613
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.459	A=0.541
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.333	A=0.667
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.11	A=0.89
HapMap	Global	Study-wide	1890	C=0.4116	A=0.5884
HapMap	American	Sub	768	C=0.336	A=0.664
HapMap	African	Sub	692	C=0.488	A=0.512
HapMap	Asian	Sub	254	C=0.437	A=0.563
HapMap	Europe	Sub	176	C=0.403	A=0.597
Korean Genome Project	KOREAN	Study-wide	1832	C=0.4973	A=0.5027
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.317	A=0.683
Northern Sweden	ACPOP	Study-wide	600	C=0.350	A=0.650
SGDP_PRJ	Global	Study-wide	480	C=0.260	A=0.740
Qatari	Global	Study-wide	216	C=0.394	A=0.606
A Vietnamese Genetic Variation Database	Global	Study-wide	210	C=0.505	A=0.495
Siberian	Global	Study-wide	50	C=0.30	A=0.70
The Danish reference pan genome	Danish	Study-wide	40	C=0.35	A=0.65
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	36	C=0.22	A=0.78

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 4	NC_000004.12:g.86310615C>A
GRCh38.p14 chr 4	NC_000004.12:g.86310615C>T
GRCh37.p13 chr 4	NC_000004.11:g.87231768C>A
GRCh37.p13 chr 4	NC_000004.11:g.87231768C>T
MAPK10 RefSeqGene	NG_013325.2:g.147516G>T
MAPK10 RefSeqGene	NG_013325.2:g.147516G>A

Gene: MAPK10, mitogen-activated protein kinase 10 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAPK10 transcript variant 5	NM_001318067.1:c.-7+43915… NM_001318067.1:c.-7+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 6	NM_001318068.1:c.-383+439… NM_001318068.1:c.-383+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 1	NM_001318069.2:c.-7+43915… NM_001318069.2:c.-7+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 7	NM_001351624.2:c.-138+439… NM_001351624.2:c.-138+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 8	NM_001351625.3:c.-138+439… NM_001351625.3:c.-138+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 9	NM_001363657.3:c.-148+439… NM_001363657.3:c.-148+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 2	NM_002753.6:c.-7+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 3	NM_138980.4:c.-148+43915G… NM_138980.4:c.-148+43915G>T	N/A	Intron Variant
MAPK10 transcript variant 1	NM_138982.4:c.-7+43915G>T	N/A	Intron Variant
MAPK10 transcript variant X1	XM_047415964.1:c.37-11620… XM_047415964.1:c.37-116208G>T	N/A	Intron Variant
MAPK10 transcript variant X2	XM_047415965.1:c.37-11620… XM_047415965.1:c.37-116208G>T	N/A	Intron Variant
MAPK10 transcript variant X3	XM_047415966.1:c.37-11620… XM_047415966.1:c.37-116208G>T	N/A	Intron Variant
MAPK10 transcript variant X4	XM_047415967.1:c.37-11620… XM_047415967.1:c.37-116208G>T	N/A	Intron Variant
MAPK10 transcript variant X5	XM_047415968.1:c.37-11620… XM_047415968.1:c.37-116208G>T	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	C=	A	T
GRCh38.p14 chr 4	NC_000004.12:g.86310615=	NC_000004.12:g.86310615C>A	NC_000004.12:g.86310615C>T
GRCh37.p13 chr 4	NC_000004.11:g.87231768=	NC_000004.11:g.87231768C>A	NC_000004.11:g.87231768C>T
MAPK10 RefSeqGene	NG_013325.2:g.147516=	NG_013325.2:g.147516G>T	NG_013325.2:g.147516G>A
MAPK10 transcript variant 5	NM_001318067.1:c.-7+43915=	NM_001318067.1:c.-7+43915G>T	NM_001318067.1:c.-7+43915G>A
MAPK10 transcript variant 6	NM_001318068.1:c.-383+43915=	NM_001318068.1:c.-383+43915G>T	NM_001318068.1:c.-383+43915G>A
MAPK10 transcript variant 1	NM_001318069.2:c.-7+43915=	NM_001318069.2:c.-7+43915G>T	NM_001318069.2:c.-7+43915G>A
MAPK10 transcript variant 7	NM_001351624.2:c.-138+43915=	NM_001351624.2:c.-138+43915G>T	NM_001351624.2:c.-138+43915G>A
MAPK10 transcript variant 8	NM_001351625.3:c.-138+43915=	NM_001351625.3:c.-138+43915G>T	NM_001351625.3:c.-138+43915G>A
MAPK10 transcript variant 9	NM_001363657.3:c.-148+43915=	NM_001363657.3:c.-148+43915G>T	NM_001363657.3:c.-148+43915G>A
MAPK10 transcript variant 1	NM_002753.3:c.-7+43915=	NM_002753.3:c.-7+43915G>T	NM_002753.3:c.-7+43915G>A
MAPK10 transcript variant 2	NM_002753.6:c.-7+43915=	NM_002753.6:c.-7+43915G>T	NM_002753.6:c.-7+43915G>A
MAPK10 transcript variant 3	NM_138980.2:c.-148+43915=	NM_138980.2:c.-148+43915G>T	NM_138980.2:c.-148+43915G>A
MAPK10 transcript variant 3	NM_138980.4:c.-148+43915=	NM_138980.4:c.-148+43915G>T	NM_138980.4:c.-148+43915G>A
MAPK10 transcript variant 2	NM_138982.2:c.-7+43915=	NM_138982.2:c.-7+43915G>T	NM_138982.2:c.-7+43915G>A
MAPK10 transcript variant 1	NM_138982.4:c.-7+43915=	NM_138982.4:c.-7+43915G>T	NM_138982.4:c.-7+43915G>A
MAPK10 transcript variant X1	XM_005263128.1:c.3+49043=	XM_005263128.1:c.3+49043G>T	XM_005263128.1:c.3+49043G>A
MAPK10 transcript variant X2	XM_005263129.1:c.-7+43915=	XM_005263129.1:c.-7+43915G>T	XM_005263129.1:c.-7+43915G>A
MAPK10 transcript variant X4	XM_005263130.1:c.-7+43915=	XM_005263130.1:c.-7+43915G>T	XM_005263130.1:c.-7+43915G>A
MAPK10 transcript variant X4	XM_005263131.1:c.-7+43915=	XM_005263131.1:c.-7+43915G>T	XM_005263131.1:c.-7+43915G>A
MAPK10 transcript variant X5	XM_005263132.1:c.-148+43915=	XM_005263132.1:c.-148+43915G>T	XM_005263132.1:c.-148+43915G>A
MAPK10 transcript variant X6	XM_005263133.1:c.3+49043=	XM_005263133.1:c.3+49043G>T	XM_005263133.1:c.3+49043G>A
MAPK10 transcript variant X7	XM_005263134.1:c.3+49043=	XM_005263134.1:c.3+49043G>T	XM_005263134.1:c.3+49043G>A
MAPK10 transcript variant X8	XM_005263135.1:c.-7+43915=	XM_005263135.1:c.-7+43915G>T	XM_005263135.1:c.-7+43915G>A
MAPK10 transcript variant X1	XM_047415964.1:c.37-116208=	XM_047415964.1:c.37-116208G>T	XM_047415964.1:c.37-116208G>A
MAPK10 transcript variant X2	XM_047415965.1:c.37-116208=	XM_047415965.1:c.37-116208G>T	XM_047415965.1:c.37-116208G>A
MAPK10 transcript variant X3	XM_047415966.1:c.37-116208=	XM_047415966.1:c.37-116208G>T	XM_047415966.1:c.37-116208G>A
MAPK10 transcript variant X4	XM_047415967.1:c.37-116208=	XM_047415967.1:c.37-116208G>T	XM_047415967.1:c.37-116208G>A
MAPK10 transcript variant X5	XM_047415968.1:c.37-116208=	XM_047415968.1:c.37-116208G>T	XM_047415968.1:c.37-116208G>A

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#.

123 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss11613955	Jul 11, 2003 (116)
2	PERLEGEN	ss14917856	Dec 05, 2003 (119)
3	CSHL-HAPMAP	ss17811015	Feb 27, 2004 (120)
4	SSAHASNP	ss22117635	Apr 05, 2004 (121)
5	PERLEGEN	ss23843448	Sep 20, 2004 (123)
6	ABI	ss44528874	Mar 15, 2006 (126)
7	AFFY	ss66015053	Dec 02, 2006 (127)
8	ILLUMINA	ss67813366	Dec 02, 2006 (127)
9	ILLUMINA	ss67980418	Dec 02, 2006 (127)
10	ILLUMINA	ss68282655	Dec 12, 2006 (127)
11	ILLUMINA	ss70941135	May 27, 2008 (130)
12	ILLUMINA	ss71544932	May 18, 2007 (127)
13	ILLUMINA	ss75483516	Dec 07, 2007 (129)
14	HGSV	ss79035639	Dec 07, 2007 (129)
15	KRIBB_YJKIM	ss84699895	Dec 16, 2007 (130)
16	BCMHGSC_JDW	ss92673526	Mar 24, 2008 (129)
17	HUMANGENOME_JCVI	ss98978448	Feb 06, 2009 (130)
18	1000GENOMES	ss108111192	Jan 22, 2009 (130)
19	1000GENOMES	ss110161281	Jan 24, 2009 (130)
20	ILLUMINA-UK	ss117079992	Feb 14, 2009 (130)
21	ENSEMBL	ss139739085	Dec 01, 2009 (131)
22	ILLUMINA	ss154438018	Dec 01, 2009 (131)
23	ILLUMINA	ss159613007	Dec 01, 2009 (131)
24	ILLUMINA	ss160900417	Dec 01, 2009 (131)
25	COMPLETE_GENOMICS	ss162317442	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss163748762	Jul 04, 2010 (132)
27	COMPLETE_GENOMICS	ss166851361	Jul 04, 2010 (132)
28	ILLUMINA	ss174477455	Jul 04, 2010 (132)
29	BUSHMAN	ss198811020	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss206504013	Jul 04, 2010 (132)
31	1000GENOMES	ss221050177	Jul 14, 2010 (132)
32	1000GENOMES	ss232480426	Jul 14, 2010 (132)
33	1000GENOMES	ss239754802	Jul 15, 2010 (132)
34	BL	ss253310033	May 09, 2011 (134)
35	GMI	ss277811723	May 04, 2012 (137)
36	GMI	ss284952047	Apr 25, 2013 (138)
37	PJP	ss293119583	May 09, 2011 (134)
38	ILLUMINA	ss481632926	May 04, 2012 (137)
39	ILLUMINA	ss481663321	May 04, 2012 (137)
40	ILLUMINA	ss482630177	Sep 08, 2015 (146)
41	ILLUMINA	ss485611247	May 04, 2012 (137)
42	ILLUMINA	ss537497154	Sep 08, 2015 (146)
43	TISHKOFF	ss557663448	Apr 25, 2013 (138)
44	SSMP	ss651468120	Apr 25, 2013 (138)
45	ILLUMINA	ss778610461	Sep 08, 2015 (146)
46	ILLUMINA	ss783251235	Sep 08, 2015 (146)
47	ILLUMINA	ss784204834	Sep 08, 2015 (146)
48	ILLUMINA	ss832511989	Sep 08, 2015 (146)
49	ILLUMINA	ss833123964	Jul 13, 2019 (153)
50	ILLUMINA	ss834067855	Sep 08, 2015 (146)
51	EVA-GONL	ss980349373	Aug 21, 2014 (142)
52	JMKIDD_LAB	ss1071714786	Aug 21, 2014 (142)
53	1000GENOMES	ss1310618719	Aug 21, 2014 (142)
54	DDI	ss1429955596	Apr 01, 2015 (144)
55	EVA_GENOME_DK	ss1580650637	Apr 01, 2015 (144)
56	EVA_DECODE	ss1589851365	Apr 01, 2015 (144)
57	EVA_UK10K_ALSPAC	ss1610545043	Apr 01, 2015 (144)
58	EVA_UK10K_TWINSUK	ss1653539076	Apr 01, 2015 (144)
59	EVA_SVP	ss1712687317	Apr 01, 2015 (144)
60	ILLUMINA	ss1752535631	Sep 08, 2015 (146)
61	HAMMER_LAB	ss1801784273	Sep 08, 2015 (146)
62	WEILL_CORNELL_DGM	ss1923593696	Feb 12, 2016 (147)
63	GENOMED	ss1969797031	Jul 19, 2016 (147)
64	JJLAB	ss2022381771	Sep 14, 2016 (149)
65	USC_VALOUEV	ss2150511143	Dec 20, 2016 (150)
66	HUMAN_LONGEVITY	ss2264659926	Dec 20, 2016 (150)
67	SYSTEMSBIOZJU	ss2625693138	Nov 08, 2017 (151)
68	ILLUMINA	ss2634144593	Nov 08, 2017 (151)
69	GRF	ss2705987318	Nov 08, 2017 (151)
70	GNOMAD	ss2811811366	Nov 08, 2017 (151)
71	SWEGEN	ss2995061452	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3024966879	Nov 08, 2017 (151)
73	CSHL	ss3345821266	Nov 08, 2017 (151)
74	ILLUMINA	ss3629008274	Oct 12, 2018 (152)
75	ILLUMINA	ss3632079520	Oct 12, 2018 (152)
76	ILLUMINA	ss3633340778	Oct 12, 2018 (152)
77	ILLUMINA	ss3634059976	Oct 12, 2018 (152)
78	ILLUMINA	ss3634960073	Oct 12, 2018 (152)
79	ILLUMINA	ss3635742756	Oct 12, 2018 (152)
80	ILLUMINA	ss3636664012	Oct 12, 2018 (152)
81	ILLUMINA	ss3637495284	Oct 12, 2018 (152)
82	ILLUMINA	ss3638497201	Oct 12, 2018 (152)
83	ILLUMINA	ss3639251073	Oct 12, 2018 (152)
84	ILLUMINA	ss3639924254	Oct 12, 2018 (152)
85	ILLUMINA	ss3640667367	Oct 12, 2018 (152)
86	ILLUMINA	ss3643447753	Oct 12, 2018 (152)
87	ILLUMINA	ss3643970399	Oct 12, 2018 (152)
88	URBANLAB	ss3647783145	Oct 12, 2018 (152)
89	EGCUT_WGS	ss3662947631	Jul 13, 2019 (153)
90	EVA_DECODE	ss3712479156	Jul 13, 2019 (153)
91	ACPOP	ss3731342578	Jul 13, 2019 (153)
92	ILLUMINA	ss3745260360	Jul 13, 2019 (153)
93	EVA	ss3762062408	Jul 13, 2019 (153)
94	ILLUMINA	ss3772754910	Jul 13, 2019 (153)
95	PACBIO	ss3784778501	Jul 13, 2019 (153)
96	PACBIO	ss3790226994	Jul 13, 2019 (153)
97	PACBIO	ss3795102356	Jul 13, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3805207745	Jul 13, 2019 (153)
99	EVA	ss3828656942	Apr 26, 2020 (154)
100	EVA	ss3837769774	Apr 26, 2020 (154)
101	EVA	ss3843207675	Apr 26, 2020 (154)
102	HGDP	ss3847756338	Apr 26, 2020 (154)
103	SGDP_PRJ	ss3859420952	Apr 26, 2020 (154)
104	KRGDB	ss3905688616	Apr 26, 2020 (154)
105	KOGIC	ss3954580628	Apr 26, 2020 (154)
106	EVA	ss3985080860	Apr 27, 2021 (155)
107	EVA	ss4017155439	Apr 27, 2021 (155)
108	TOPMED	ss4621431574	Apr 27, 2021 (155)
109	TOMMO_GENOMICS	ss5166682522	Apr 27, 2021 (155)
110	1000G_HIGH_COVERAGE	ss5259970375	Oct 17, 2022 (156)
111	EVA	ss5314972065	Oct 17, 2022 (156)
112	EVA	ss5350396800	Oct 17, 2022 (156)
113	HUGCELL_USP	ss5458646713	Oct 17, 2022 (156)
114	EVA	ss5507603369	Oct 17, 2022 (156)
115	1000G_HIGH_COVERAGE	ss5541460747	Oct 17, 2022 (156)
116	SANFORD_IMAGENETICS	ss5635482581	Oct 17, 2022 (156)
117	TOMMO_GENOMICS	ss5701300474	Oct 17, 2022 (156)
118	EVA	ss5799620043	Oct 17, 2022 (156)
119	YY_MCH	ss5805277278	Oct 17, 2022 (156)
120	EVA	ss5844297017	Oct 17, 2022 (156)
121	EVA	ss5854318776	Oct 17, 2022 (156)
122	EVA	ss5864317619	Oct 17, 2022 (156)
123	EVA	ss5963866138	Oct 17, 2022 (156)
124	1000Genomes	NC_000004.11 - 87231768	Oct 12, 2018 (152)
125	1000Genomes_30x	NC_000004.12 - 86310615	Oct 17, 2022 (156)
126	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 87231768	Oct 12, 2018 (152)
127	Genetic variation in the Estonian population	NC_000004.11 - 87231768	Oct 12, 2018 (152)
128	The Danish reference pan genome	NC_000004.11 - 87231768	Apr 26, 2020 (154)
129	gnomAD - Genomes	NC_000004.12 - 86310615	Apr 27, 2021 (155)
130	Genome of the Netherlands Release 5	NC_000004.11 - 87231768	Apr 26, 2020 (154)
131	HGDP-CEPH-db Supplement 1	NC_000004.10 - 87450792	Apr 26, 2020 (154)
132	HapMap	NC_000004.12 - 86310615	Apr 26, 2020 (154)
133	KOREAN population from KRGDB	NC_000004.11 - 87231768	Apr 26, 2020 (154)
134	Korean Genome Project	NC_000004.12 - 86310615	Apr 26, 2020 (154)
135	Northern Sweden	NC_000004.11 - 87231768	Jul 13, 2019 (153)
136	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 87231768	Apr 27, 2021 (155)
137	Qatari	NC_000004.11 - 87231768	Apr 26, 2020 (154)
138	SGDP_PRJ	NC_000004.11 - 87231768	Apr 26, 2020 (154)
139	Siberian	NC_000004.11 - 87231768	Apr 26, 2020 (154)
140	8.3KJPN	NC_000004.11 - 87231768	Apr 27, 2021 (155)
141	14KJPN	NC_000004.12 - 86310615	Oct 17, 2022 (156)
142	TopMed	NC_000004.12 - 86310615	Apr 27, 2021 (155)
143	UK 10K study - Twins	NC_000004.11 - 87231768	Oct 12, 2018 (152)
144	A Vietnamese Genetic Variation Database	NC_000004.11 - 87231768	Jul 13, 2019 (153)
145	ALFA	NC_000004.12 - 86310615	Apr 27, 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)
rs61556721	May 27, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss79035639, ss3639251073, ss3639924254, ss3643970399	NC_000004.9:87588946:C:A	NC_000004.12:86310614:C:A	(self)
434230, ss92673526, ss108111192, ss110161281, ss117079992, ss162317442, ss163748762, ss166851361, ss198811020, ss206504013, ss253310033, ss277811723, ss284952047, ss293119583, ss481632926, ss1589851365, ss1712687317, ss3643447753, ss3847756338	NC_000004.10:87450791:C:A	NC_000004.12:86310614:C:A	(self)
22046520, 12262272, 8685879, 6815576, 5415142, 12866010, 4627443, 306787, 5635626, 11437932, 3027497, 24651829, 12262272, 2698473, ss221050177, ss232480426, ss239754802, ss481663321, ss482630177, ss485611247, ss537497154, ss557663448, ss651468120, ss778610461, ss783251235, ss784204834, ss832511989, ss833123964, ss834067855, ss980349373, ss1071714786, ss1310618719, ss1429955596, ss1580650637, ss1610545043, ss1653539076, ss1752535631, ss1801784273, ss1923593696, ss1969797031, ss2022381771, ss2150511143, ss2625693138, ss2634144593, ss2705987318, ss2811811366, ss2995061452, ss3345821266, ss3629008274, ss3632079520, ss3633340778, ss3634059976, ss3634960073, ss3635742756, ss3636664012, ss3637495284, ss3638497201, ss3640667367, ss3662947631, ss3731342578, ss3745260360, ss3762062408, ss3772754910, ss3784778501, ss3790226994, ss3795102356, ss3828656942, ss3837769774, ss3859420952, ss3905688616, ss3985080860, ss4017155439, ss5166682522, ss5314972065, ss5350396800, ss5507603369, ss5635482581, ss5799620043, ss5844297017, ss5963866138	NC_000004.11:87231767:C:A	NC_000004.12:86310614:C:A	(self)
28986682, 156154066, 2654392, 10958629, 35137578, 458809130, 3162601909, ss2264659926, ss3024966879, ss3647783145, ss3712479156, ss3805207745, ss3843207675, ss3954580628, ss4621431574, ss5259970375, ss5458646713, ss5541460747, ss5701300474, ss5805277278, ss5854318776, ss5864317619	NC_000004.12:86310614:C:A	NC_000004.12:86310614:C:A	(self)
ss11613955	NT_016354.15:11726472:C:A	NC_000004.12:86310614:C:A	(self)
ss17811015, ss22117635	NT_016354.16:11726472:C:A	NC_000004.12:86310614:C:A	(self)
ss14917856, ss23843448, ss44528874, ss66015053, ss67813366, ss67980418, ss68282655, ss70941135, ss71544932, ss75483516, ss84699895, ss98978448, ss139739085, ss154438018, ss159613007, ss160900417, ss174477455	NT_016354.19:11779488:C:A	NC_000004.12:86310614:C:A	(self)
12866010, ss3905688616	NC_000004.11:87231767:C:T	NC_000004.12:86310614:C:T	(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 rs7655217

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

rs7655217