Name: rs10851643
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.

rs10851643

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:59102985 (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>C / A>G / A>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.340138 (102253/300622, ALFA)
C=0.363229 (96143/264690, TOPMED)
C=0.353043 (49385/139884, GnomAD) (+ 21 more)
C=0.40789 (32102/78702, PAGE_STUDY)
C=0.45700 (12913/28256, 14KJPN)
C=0.45758 (7669/16760, 8.3KJPN)
C=0.3518 (2253/6404, 1000G_30x)
C=0.3532 (1769/5008, 1000G)
C=0.3092 (1385/4480, Estonian)
C=0.3158 (1217/3854, ALSPAC)
C=0.3056 (1133/3708, TWINSUK)
C=0.4536 (1329/2930, KOREAN)
C=0.4131 (861/2084, HGDP_Stanford)
C=0.3478 (658/1892, HapMap)
C=0.4940 (905/1832, Korea1K)
C=0.333 (332/998, GoNL)
C=0.489 (385/788, PRJEB37584)
C=0.312 (187/600, NorthernSweden)
A=0.372 (134/360, SGDP_PRJ)
C=0.361 (78/216, Qatari)
C=0.401 (85/212, Vietnamese)
C=0.26 (12/46, Ancient Sardinia)
C=0.35 (14/40, GENOME_DK)
A=0.42 (15/36, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 1 citation
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	305658	A=0.659767	C=0.340233
European	Sub	268798	A=0.665924	C=0.334076
African	Sub	9514	A=0.6498	C=0.3502
African Others	Sub	372	A=0.629	C=0.371
African American	Sub	9142	A=0.6506	C=0.3494
Asian	Sub	3942	A=0.5170	C=0.4830
East Asian	Sub	3196	A=0.5269	C=0.4731
Other Asian	Sub	746	A=0.475	C=0.525
Latin American 1	Sub	1134	A=0.6111	C=0.3889
Latin American 2	Sub	7214	A=0.5123	C=0.4877
South Asian	Sub	5224	A=0.7423	C=0.2577
Other	Sub	9832	A=0.6283	C=0.3717

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
Allele Frequency Aggregator	Total	Global	300622	A=0.659862	C=0.340138
Allele Frequency Aggregator	European	Sub	265704	A=0.665918	C=0.334082
Allele Frequency Aggregator	Other	Sub	9032	A=0.6306	C=0.3694
Allele Frequency Aggregator	African	Sub	8372	A=0.6487	C=0.3513
Allele Frequency Aggregator	Latin American 2	Sub	7214	A=0.5123	C=0.4877
Allele Frequency Aggregator	South Asian	Sub	5224	A=0.7423	C=0.2577
Allele Frequency Aggregator	Asian	Sub	3942	A=0.5170	C=0.4830
Allele Frequency Aggregator	Latin American 1	Sub	1134	A=0.6111	C=0.3889
TopMed	Global	Study-wide	264690	A=0.636771	C=0.363229
gnomAD - Genomes	Global	Study-wide	139884	A=0.646957	C=0.353043
gnomAD - Genomes	European	Sub	75756	A=0.66568	C=0.33432
gnomAD - Genomes	African	Sub	41900	A=0.64475	C=0.35525
gnomAD - Genomes	American	Sub	13638	A=0.58271	C=0.41729
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	A=0.6194	C=0.3806
gnomAD - Genomes	East Asian	Sub	3120	A=0.5410	C=0.4590
gnomAD - Genomes	Other	Sub	2146	A=0.6342	C=0.3658
The PAGE Study	Global	Study-wide	78702	A=0.59211	C=0.40789
The PAGE Study	AfricanAmerican	Sub	32516	A=0.64485	C=0.35515
The PAGE Study	Mexican	Sub	10810	A=0.49593	C=0.50407
The PAGE Study	Asian	Sub	8318	A=0.5424	C=0.4576
The PAGE Study	PuertoRican	Sub	7918	A=0.6123	C=0.3877
The PAGE Study	NativeHawaiian	Sub	4534	A=0.4411	C=0.5589
The PAGE Study	Cuban	Sub	4230	A=0.6288	C=0.3712
The PAGE Study	Dominican	Sub	3828	A=0.6429	C=0.3571
The PAGE Study	CentralAmerican	Sub	2450	A=0.5396	C=0.4604
The PAGE Study	SouthAmerican	Sub	1982	A=0.5333	C=0.4667
The PAGE Study	NativeAmerican	Sub	1260	A=0.6032	C=0.3968
The PAGE Study	SouthAsian	Sub	856	A=0.761	C=0.239
14KJPN	JAPANESE	Study-wide	28256	A=0.54300	C=0.45700
8.3KJPN	JAPANESE	Study-wide	16760	A=0.54242	C=0.45758
1000Genomes_30x	Global	Study-wide	6404	A=0.6482	C=0.3518
1000Genomes_30x	African	Sub	1786	A=0.6585	C=0.3415
1000Genomes_30x	Europe	Sub	1266	A=0.7022	C=0.2978
1000Genomes_30x	South Asian	Sub	1202	A=0.7546	C=0.2454
1000Genomes_30x	East Asian	Sub	1170	A=0.5547	C=0.4453
1000Genomes_30x	American	Sub	980	A=0.541	C=0.459
1000Genomes	Global	Study-wide	5008	A=0.6468	C=0.3532
1000Genomes	African	Sub	1322	A=0.6475	C=0.3525
1000Genomes	East Asian	Sub	1008	A=0.5516	C=0.4484
1000Genomes	Europe	Sub	1006	A=0.6998	C=0.3002
1000Genomes	South Asian	Sub	978	A=0.770	C=0.230
1000Genomes	American	Sub	694	A=0.533	C=0.467
Genetic variation in the Estonian population	Estonian	Study-wide	4480	A=0.6908	C=0.3092
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.6842	C=0.3158
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.6944	C=0.3056
KOREAN population from KRGDB	KOREAN	Study-wide	2930	A=0.5464	C=0.4536, G=0.0000, T=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	A=0.5869	C=0.4131
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	A=0.572	C=0.428
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	A=0.659	C=0.341
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	A=0.551	C=0.449
HGDP-CEPH-db Supplement 1	Europe	Sub	320	A=0.622	C=0.378
HGDP-CEPH-db Supplement 1	Africa	Sub	242	A=0.653	C=0.347
HGDP-CEPH-db Supplement 1	America	Sub	216	A=0.435	C=0.565
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	A=0.51	C=0.49
HapMap	Global	Study-wide	1892	A=0.6522	C=0.3478
HapMap	American	Sub	770	A=0.671	C=0.329
HapMap	African	Sub	692	A=0.675	C=0.325
HapMap	Asian	Sub	254	A=0.551	C=0.449
HapMap	Europe	Sub	176	A=0.625	C=0.375
Korean Genome Project	KOREAN	Study-wide	1832	A=0.5060	C=0.4940
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	A=0.667	C=0.333
CNV burdens in cranial meningiomas	Global	Study-wide	788	A=0.511	C=0.489
CNV burdens in cranial meningiomas	CRM	Sub	788	A=0.511	C=0.489
Northern Sweden	ACPOP	Study-wide	600	A=0.688	C=0.312
SGDP_PRJ	Global	Study-wide	360	A=0.372	C=0.628
Qatari	Global	Study-wide	216	A=0.639	C=0.361
A Vietnamese Genetic Variation Database	Global	Study-wide	212	A=0.599	C=0.401
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	46	A=0.74	C=0.26
The Danish reference pan genome	Danish	Study-wide	40	A=0.65	C=0.35
Siberian	Global	Study-wide	36	A=0.42	C=0.58

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 15	NC_000015.10:g.59102985A>C
GRCh38.p14 chr 15	NC_000015.10:g.59102985A>G
GRCh38.p14 chr 15	NC_000015.10:g.59102985A>T
GRCh37.p13 chr 15	NC_000015.9:g.59395184A>C
GRCh37.p13 chr 15	NC_000015.9:g.59395184A>G
GRCh37.p13 chr 15	NC_000015.9:g.59395184A>T

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=	C	G	T
GRCh38.p14 chr 15	NC_000015.10:g.59102985=	NC_000015.10:g.59102985A>C	NC_000015.10:g.59102985A>G	NC_000015.10:g.59102985A>T
GRCh37.p13 chr 15	NC_000015.9:g.59395184=	NC_000015.9:g.59395184A>C	NC_000015.9:g.59395184A>G	NC_000015.9:g.59395184A>T

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#.

135 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss16206705	Feb 27, 2004 (120)
2	SC_SNP	ss18304218	Feb 27, 2004 (120)
3	SC_SNP	ss18551256	Feb 27, 2004 (120)
4	SSAHASNP	ss21228841	Apr 05, 2004 (121)
5	ABI	ss43696036	Mar 14, 2006 (126)
6	ILLUMINA	ss65794762	Oct 16, 2006 (127)
7	ILLUMINA	ss66699206	Dec 01, 2006 (127)
8	ILLUMINA	ss66905100	Dec 01, 2006 (127)
9	ILLUMINA	ss67029194	Dec 01, 2006 (127)
10	ILLUMINA	ss70382073	May 18, 2007 (127)
11	ILLUMINA	ss70502598	May 25, 2008 (130)
12	ILLUMINA	ss71028723	May 18, 2007 (127)
13	ILLUMINA	ss75636040	Dec 07, 2007 (129)
14	HGSV	ss81060730	Dec 15, 2007 (130)
15	HGSV	ss81106733	Dec 15, 2007 (130)
16	HGSV	ss84154596	Dec 15, 2007 (130)
17	KRIBB_YJKIM	ss85015224	Dec 15, 2007 (130)
18	BGI	ss103244149	Dec 01, 2009 (131)
19	1000GENOMES	ss114250667	Jan 25, 2009 (130)
20	ILLUMINA-UK	ss118247718	Dec 01, 2009 (131)
21	ILLUMINA	ss121402329	Dec 01, 2009 (131)
22	ENSEMBL	ss136888272	Dec 01, 2009 (131)
23	ILLUMINA	ss152848537	Dec 01, 2009 (131)
24	ILLUMINA	ss159147663	Dec 01, 2009 (131)
25	ILLUMINA	ss159929540	Dec 01, 2009 (131)
26	COMPLETE_GENOMICS	ss169626692	Jul 04, 2010 (132)
27	ILLUMINA	ss169667826	Jul 04, 2010 (132)
28	ILLUMINA	ss170645099	Jul 04, 2010 (132)
29	BUSHMAN	ss200908102	Jul 04, 2010 (132)
30	BCM-HGSC-SUB	ss207243904	Jul 04, 2010 (132)
31	1000GENOMES	ss226921001	Jul 14, 2010 (132)
32	1000GENOMES	ss236799060	Jul 15, 2010 (132)
33	1000GENOMES	ss243182744	Jul 15, 2010 (132)
34	GMI	ss282278453	May 04, 2012 (137)
35	GMI	ss286963452	Apr 25, 2013 (138)
36	PJP	ss291731456	May 09, 2011 (134)
37	ILLUMINA	ss479376639	May 04, 2012 (137)
38	ILLUMINA	ss479379804	May 04, 2012 (137)
39	ILLUMINA	ss479784003	Sep 08, 2015 (146)
40	ILLUMINA	ss484488435	May 04, 2012 (137)
41	ILLUMINA	ss536643811	Sep 08, 2015 (146)
42	TISHKOFF	ss564513559	Apr 25, 2013 (138)
43	SSMP	ss660244196	Apr 25, 2013 (138)
44	ILLUMINA	ss778743149	Aug 21, 2014 (142)
45	ILLUMINA	ss782690746	Aug 21, 2014 (142)
46	ILLUMINA	ss783659021	Aug 21, 2014 (142)
47	ILLUMINA	ss825351624	Apr 01, 2015 (144)
48	ILLUMINA	ss831941711	Apr 01, 2015 (144)
49	ILLUMINA	ss832660290	Aug 21, 2014 (142)
50	ILLUMINA	ss833250979	Aug 21, 2014 (142)
51	ILLUMINA	ss834202753	Aug 21, 2014 (142)
52	EVA-GONL	ss991842867	Aug 21, 2014 (142)
53	JMKIDD_LAB	ss1080170152	Aug 21, 2014 (142)
54	1000GENOMES	ss1353683801	Aug 21, 2014 (142)
55	DDI	ss1427642960	Apr 01, 2015 (144)
56	EVA_GENOME_DK	ss1577650378	Apr 01, 2015 (144)
57	EVA_UK10K_ALSPAC	ss1633114521	Apr 01, 2015 (144)
58	EVA_UK10K_TWINSUK	ss1676108554	Apr 01, 2015 (144)
59	EVA_DECODE	ss1695863121	Apr 01, 2015 (144)
60	EVA_SVP	ss1713494103	Apr 01, 2015 (144)
61	ILLUMINA	ss1752165788	Sep 08, 2015 (146)
62	HAMMER_LAB	ss1808228774	Sep 08, 2015 (146)
63	WEILL_CORNELL_DGM	ss1935248875	Feb 12, 2016 (147)
64	ILLUMINA	ss1946395293	Feb 12, 2016 (147)
65	ILLUMINA	ss1959616875	Feb 12, 2016 (147)
66	GENOMED	ss1968122121	Jul 19, 2016 (147)
67	JJLAB	ss2028404770	Sep 14, 2016 (149)
68	USC_VALOUEV	ss2156808961	Dec 20, 2016 (150)
69	HUMAN_LONGEVITY	ss2207235411	Dec 20, 2016 (150)
70	SYSTEMSBIOZJU	ss2628697305	Nov 08, 2017 (151)
71	ILLUMINA	ss2633236502	Nov 08, 2017 (151)
72	GRF	ss2701282063	Nov 08, 2017 (151)
73	ILLUMINA	ss2710817932	Nov 08, 2017 (151)
74	GNOMAD	ss2935528585	Nov 08, 2017 (151)
75	SWEGEN	ss3013371915	Nov 08, 2017 (151)
76	ILLUMINA	ss3021638108	Nov 08, 2017 (151)
77	BIOINF_KMB_FNS_UNIBA	ss3028026271	Nov 08, 2017 (151)
78	CSHL	ss3351141097	Nov 08, 2017 (151)
79	ILLUMINA	ss3625674367	Oct 12, 2018 (152)
80	ILLUMINA	ss3627373771	Oct 12, 2018 (152)
81	ILLUMINA	ss3631228778	Oct 12, 2018 (152)
82	ILLUMINA	ss3633099295	Oct 12, 2018 (152)
83	ILLUMINA	ss3633803973	Oct 12, 2018 (152)
84	ILLUMINA	ss3634609355	Oct 12, 2018 (152)
85	ILLUMINA	ss3635492841	Oct 12, 2018 (152)
86	ILLUMINA	ss3636299273	Oct 12, 2018 (152)
87	ILLUMINA	ss3637244125	Oct 12, 2018 (152)
88	ILLUMINA	ss3638088787	Oct 12, 2018 (152)
89	ILLUMINA	ss3639057422	Oct 12, 2018 (152)
90	ILLUMINA	ss3639534048	Oct 12, 2018 (152)
91	ILLUMINA	ss3640316676	Oct 12, 2018 (152)
92	ILLUMINA	ss3643072816	Oct 12, 2018 (152)
93	ILLUMINA	ss3644648391	Oct 12, 2018 (152)
94	URBANLAB	ss3650366277	Oct 12, 2018 (152)
95	ILLUMINA	ss3652039119	Oct 12, 2018 (152)
96	EGCUT_WGS	ss3680516292	Jul 13, 2019 (153)
97	EVA_DECODE	ss3697998767	Jul 13, 2019 (153)
98	ILLUMINA	ss3725504260	Jul 13, 2019 (153)
99	ACPOP	ss3740971916	Jul 13, 2019 (153)
100	ILLUMINA	ss3744131893	Jul 13, 2019 (153)
101	ILLUMINA	ss3744909872	Jul 13, 2019 (153)
102	EVA	ss3753154417	Jul 13, 2019 (153)
103	PAGE_CC	ss3771833619	Jul 13, 2019 (153)
104	ILLUMINA	ss3772408525	Jul 13, 2019 (153)
105	PACBIO	ss3787862620	Jul 13, 2019 (153)
106	PACBIO	ss3792872280	Jul 13, 2019 (153)
107	PACBIO	ss3797756864	Jul 13, 2019 (153)
108	KHV_HUMAN_GENOMES	ss3818471278	Jul 13, 2019 (153)
109	EVA	ss3834263224	Apr 27, 2020 (154)
110	EVA	ss3840730205	Apr 27, 2020 (154)
111	EVA	ss3846219171	Apr 27, 2020 (154)
112	HGDP	ss3847525448	Apr 27, 2020 (154)
113	SGDP_PRJ	ss3883031825	Apr 27, 2020 (154)
114	KRGDB	ss3932212341	Apr 27, 2020 (154)
115	KOGIC	ss3976249692	Apr 27, 2020 (154)
116	EVA	ss3984702216	Apr 27, 2021 (155)
117	EVA	ss3985719883	Apr 27, 2021 (155)
118	EVA	ss4017704704	Apr 27, 2021 (155)
119	TOPMED	ss4993310695	Apr 27, 2021 (155)
120	TOMMO_GENOMICS	ss5216446886	Apr 27, 2021 (155)
121	1000G_HIGH_COVERAGE	ss5298634080	Oct 16, 2022 (156)
122	EVA	ss5315788369	Oct 16, 2022 (156)
123	EVA	ss5419582936	Oct 16, 2022 (156)
124	HUGCELL_USP	ss5492342129	Oct 16, 2022 (156)
125	EVA	ss5511451953	Oct 16, 2022 (156)
126	1000G_HIGH_COVERAGE	ss5600133873	Oct 16, 2022 (156)
127	SANFORD_IMAGENETICS	ss5657620925	Oct 16, 2022 (156)
128	TOMMO_GENOMICS	ss5770325328	Oct 16, 2022 (156)
129	EVA	ss5799939440	Oct 16, 2022 (156)
130	YY_MCH	ss5815383936	Oct 16, 2022 (156)
131	EVA	ss5828276219	Oct 16, 2022 (156)
132	EVA	ss5847745148	Oct 16, 2022 (156)
133	EVA	ss5851317136	Oct 16, 2022 (156)
134	EVA	ss5876097525	Oct 16, 2022 (156)
135	EVA	ss5949026394	Oct 16, 2022 (156)
136	1000Genomes	NC_000015.9 - 59395184	Oct 12, 2018 (152)
137	1000Genomes_30x	NC_000015.10 - 59102985	Oct 16, 2022 (156)
138	The Avon Longitudinal Study of Parents and Children	NC_000015.9 - 59395184	Oct 12, 2018 (152)
139	Genetic variation in the Estonian population	NC_000015.9 - 59395184	Oct 12, 2018 (152)
140	The Danish reference pan genome	NC_000015.9 - 59395184	Apr 27, 2020 (154)
141	gnomAD - Genomes	NC_000015.10 - 59102985	Apr 27, 2021 (155)
142	Genome of the Netherlands Release 5	NC_000015.9 - 59395184	Apr 27, 2020 (154)
143	HGDP-CEPH-db Supplement 1	NC_000015.8 - 57182476	Apr 27, 2020 (154)
144	HapMap	NC_000015.10 - 59102985	Apr 27, 2020 (154)
145	KOREAN population from KRGDB	NC_000015.9 - 59395184	Apr 27, 2020 (154)
146	Korean Genome Project	NC_000015.10 - 59102985	Apr 27, 2020 (154)
147	Northern Sweden	NC_000015.9 - 59395184	Jul 13, 2019 (153)
148	The PAGE Study	NC_000015.10 - 59102985	Jul 13, 2019 (153)
149	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000015.9 - 59395184	Apr 27, 2021 (155)
150	CNV burdens in cranial meningiomas	NC_000015.9 - 59395184	Apr 27, 2021 (155)
151	Qatari	NC_000015.9 - 59395184	Apr 27, 2020 (154)
152	SGDP_PRJ	NC_000015.9 - 59395184	Apr 27, 2020 (154)
153	Siberian	NC_000015.9 - 59395184	Apr 27, 2020 (154)
154	8.3KJPN	NC_000015.9 - 59395184	Apr 27, 2021 (155)
155	14KJPN	NC_000015.10 - 59102985	Oct 16, 2022 (156)
156	TopMed	NC_000015.10 - 59102985	Apr 27, 2021 (155)
157	UK 10K study - Twins	NC_000015.9 - 59395184	Oct 12, 2018 (152)
158	A Vietnamese Genetic Variation Database	NC_000015.9 - 59395184	Jul 13, 2019 (153)
159	ALFA	NC_000015.10 - 59102985	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)
rs59363670	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
203340, ss81060730, ss81106733, ss84154596, ss114250667, ss118247718, ss159929540, ss169626692, ss200908102, ss207243904, ss282278453, ss286963452, ss291731456, ss479376639, ss825351624, ss1695863121, ss1713494103, ss3639057422, ss3639534048, ss3643072816, ss3847525448	NC_000015.8:57182475:A:C	NC_000015.10:59102984:A:C	(self)
66763465, 37064347, 26254540, 3880075, 16549861, 39389735, 14256781, 945810, 251738, 17290805, 35048805, 9325315, 74416193, 37064347, 8247615, ss226921001, ss236799060, ss243182744, ss479379804, ss479784003, ss484488435, ss536643811, ss564513559, ss660244196, ss778743149, ss782690746, ss783659021, ss831941711, ss832660290, ss833250979, ss834202753, ss991842867, ss1080170152, ss1353683801, ss1427642960, ss1577650378, ss1633114521, ss1676108554, ss1752165788, ss1808228774, ss1935248875, ss1946395293, ss1959616875, ss1968122121, ss2028404770, ss2156808961, ss2628697305, ss2633236502, ss2701282063, ss2710817932, ss2935528585, ss3013371915, ss3021638108, ss3351141097, ss3625674367, ss3627373771, ss3631228778, ss3633099295, ss3633803973, ss3634609355, ss3635492841, ss3636299273, ss3637244125, ss3638088787, ss3640316676, ss3644648391, ss3652039119, ss3680516292, ss3740971916, ss3744131893, ss3744909872, ss3753154417, ss3772408525, ss3787862620, ss3792872280, ss3797756864, ss3834263224, ss3840730205, ss3883031825, ss3932212341, ss3984702216, ss3985719883, ss4017704704, ss5216446886, ss5315788369, ss5419582936, ss5511451953, ss5657620925, ss5799939440, ss5828276219, ss5847745148, ss5949026394	NC_000015.9:59395183:A:C	NC_000015.10:59102984:A:C	(self)
87659808, 470666811, 1275072, 32627693, 1055088, 104162432, 208856355, 4090994073, ss2207235411, ss3028026271, ss3650366277, ss3697998767, ss3725504260, ss3771833619, ss3818471278, ss3846219171, ss3976249692, ss4993310695, ss5298634080, ss5492342129, ss5600133873, ss5770325328, ss5815383936, ss5851317136, ss5876097525	NC_000015.10:59102984:A:C	NC_000015.10:59102984:A:C	(self)
ss16206705, ss18304218, ss18551256, ss21228841	NT_010194.16:30185740:A:C	NC_000015.10:59102984:A:C	(self)
ss43696036, ss65794762, ss66699206, ss66905100, ss67029194, ss70382073, ss70502598, ss71028723, ss75636040, ss85015224, ss103244149, ss121402329, ss136888272, ss152848537, ss159147663, ss169667826, ss170645099	NT_010194.17:30185740:A:C	NC_000015.10:59102984:A:C	(self)
39389735, ss3932212341	NC_000015.9:59395183:A:G	NC_000015.10:59102984:A:G	(self)
39389735, ss3932212341	NC_000015.9:59395183:A:T	NC_000015.10:59102984:A:T	(self)

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

1 citation for rs10851643

PMID	Title	Author	Year	Journal
21965272	Common genetic variants in cell cycle pathway are associated with survival in stage III-IV non-small-cell lung cancer.	Yin J et al.	2011	Carcinogenesis

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10851643