Name: rs10000081
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.

rs10000081

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:17346740 (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=0.345789 (91527/264690, TOPMED)
C=0.257150 (55189/214618, ALFA)
C=0.256729 (52649/205076, GENOGRAPHIC) (+ 21 more)
C=0.343652 (48081/139912, GnomAD)
C=0.42859 (12111/28258, 14KJPN)
C=0.43079 (7220/16760, 8.3KJPN)
C=0.3446 (2207/6404, 1000G_30x)
C=0.3421 (1713/5008, 1000G)
C=0.3199 (1433/4480, Estonian)
C=0.2460 (948/3854, ALSPAC)
C=0.2398 (889/3708, TWINSUK)
C=0.4229 (1239/2930, KOREAN)
C=0.3383 (705/2084, HGDP_Stanford)
C=0.3673 (695/1892, HapMap)
C=0.4143 (759/1832, Korea1K)
C=0.1840 (209/1136, Daghestan)
C=0.242 (242/998, GoNL)
C=0.250 (150/600, NorthernSweden)
C=0.208 (100/480, SGDP_PRJ)
C=0.278 (60/216, Qatari)
C=0.407 (87/214, Vietnamese)
C=0.24 (22/92, Ancient Sardinia)
C=0.18 (10/56, Siberian)
C=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	214618	C=0.257150	T=0.742850
European	Sub	188558	C=0.244477	T=0.755523
African	Sub	9726	C=0.4975	T=0.5025
African Others	Sub	348	C=0.517	T=0.483
African American	Sub	9378	C=0.4968	T=0.5032
Asian	Sub	748	C=0.406	T=0.594
East Asian	Sub	602	C=0.420	T=0.580
Other Asian	Sub	146	C=0.349	T=0.651
Latin American 1	Sub	784	C=0.330	T=0.670
Latin American 2	Sub	2842	C=0.3737	T=0.6263
South Asian	Sub	5042	C=0.1378	T=0.8622
Other	Sub	6918	C=0.2793	T=0.7207

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=0.345789	T=0.654211
Allele Frequency Aggregator	Total	Global	214618	C=0.257150	T=0.742850
Allele Frequency Aggregator	European	Sub	188558	C=0.244477	T=0.755523
Allele Frequency Aggregator	African	Sub	9726	C=0.4975	T=0.5025
Allele Frequency Aggregator	Other	Sub	6918	C=0.2793	T=0.7207
Allele Frequency Aggregator	South Asian	Sub	5042	C=0.1378	T=0.8622
Allele Frequency Aggregator	Latin American 2	Sub	2842	C=0.3737	T=0.6263
Allele Frequency Aggregator	Latin American 1	Sub	784	C=0.330	T=0.670
Allele Frequency Aggregator	Asian	Sub	748	C=0.406	T=0.594
Genographic Project	Global	Study-wide	205076	C=0.256729	T=0.743271
gnomAD - Genomes	Global	Study-wide	139912	C=0.343652	T=0.656348
gnomAD - Genomes	European	Sub	75824	C=0.26536	T=0.73464
gnomAD - Genomes	African	Sub	41900	C=0.49136	T=0.50864
gnomAD - Genomes	American	Sub	13624	C=0.34792	T=0.65208
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.1989	T=0.8011
gnomAD - Genomes	East Asian	Sub	3098	C=0.3938	T=0.6062
gnomAD - Genomes	Other	Sub	2142	C=0.3506	T=0.6494
14KJPN	JAPANESE	Study-wide	28258	C=0.42859	T=0.57141
8.3KJPN	JAPANESE	Study-wide	16760	C=0.43079	T=0.56921
1000Genomes_30x	Global	Study-wide	6404	C=0.3446	T=0.6554
1000Genomes_30x	African	Sub	1786	C=0.4978	T=0.5022
1000Genomes_30x	Europe	Sub	1266	C=0.2670	T=0.7330
1000Genomes_30x	South Asian	Sub	1202	C=0.1206	T=0.8794
1000Genomes_30x	East Asian	Sub	1170	C=0.4265	T=0.5735
1000Genomes_30x	American	Sub	980	C=0.343	T=0.657
1000Genomes	Global	Study-wide	5008	C=0.3421	T=0.6579
1000Genomes	African	Sub	1322	C=0.4947	T=0.5053
1000Genomes	East Asian	Sub	1008	C=0.4266	T=0.5734
1000Genomes	Europe	Sub	1006	C=0.2714	T=0.7286
1000Genomes	South Asian	Sub	978	C=0.120	T=0.880
1000Genomes	American	Sub	694	C=0.344	T=0.656
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.3199	T=0.6801
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.2460	T=0.7540
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.2398	T=0.7602
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.4229	A=0.0000, T=0.5771
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.3383	T=0.6617
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.451	T=0.549
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.200	T=0.800
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.277	T=0.723
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.237	T=0.762
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.393	T=0.607
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.579	T=0.421
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.24	T=0.76
HapMap	Global	Study-wide	1892	C=0.3673	T=0.6327
HapMap	American	Sub	770	C=0.286	T=0.714
HapMap	African	Sub	692	C=0.462	T=0.538
HapMap	Asian	Sub	254	C=0.457	T=0.543
HapMap	Europe	Sub	176	C=0.222	T=0.778
Korean Genome Project	KOREAN	Study-wide	1832	C=0.4143	T=0.5857
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	C=0.1840	T=0.8160
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	C=0.150	T=0.850
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	C=0.188	T=0.812
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	C=0.279	T=0.721
Genome-wide autozygosity in Daghestan	Europe	Sub	108	C=0.343	T=0.657
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	C=0.13	T=0.87
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	C=0.11	T=0.89
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.242	T=0.758
Northern Sweden	ACPOP	Study-wide	600	C=0.250	T=0.750
SGDP_PRJ	Global	Study-wide	480	C=0.208	T=0.792
Qatari	Global	Study-wide	216	C=0.278	T=0.722
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.407	T=0.593
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	92	C=0.24	T=0.76
Siberian	Global	Study-wide	56	C=0.18	T=0.82
The Danish reference pan genome	Danish	Study-wide	40	C=0.23	T=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.17346740C>A
GRCh38.p14 chr 4	NC_000004.12:g.17346740C>T
GRCh37.p13 chr 4	NC_000004.11:g.17348363C>A
GRCh37.p13 chr 4	NC_000004.11:g.17348363C>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	C=	A	T
GRCh38.p14 chr 4	NC_000004.12:g.17346740=	NC_000004.12:g.17346740C>A	NC_000004.12:g.17346740C>T
GRCh37.p13 chr 4	NC_000004.11:g.17348363=	NC_000004.11:g.17348363C>A	NC_000004.11:g.17348363C>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#.

124 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss13845725	Dec 05, 2003 (119)
2	CSHL-HAPMAP	ss19565940	Feb 27, 2004 (120)
3	CSHL-HAPMAP	ss20195305	Feb 27, 2004 (120)
4	PERLEGEN	ss23316471	Sep 20, 2004 (123)
5	ABI	ss44553534	Mar 15, 2006 (126)
6	ILLUMINA	ss66863605	Dec 01, 2006 (127)
7	ILLUMINA	ss66932304	Dec 01, 2006 (127)
8	ILLUMINA	ss68074909	Dec 12, 2006 (127)
9	ILLUMINA	ss70458953	May 23, 2008 (130)
10	ILLUMINA	ss70979495	May 18, 2007 (127)
11	ILLUMINA	ss75674072	Dec 07, 2007 (129)
12	KRIBB_YJKIM	ss84887359	Dec 14, 2007 (130)
13	BCMHGSC_JDW	ss92488256	Mar 24, 2008 (129)
14	BGI	ss104045395	Dec 01, 2009 (131)
15	1000GENOMES	ss111864469	Jan 25, 2009 (130)
16	1000GENOMES	ss112959141	Jan 25, 2009 (130)
17	ENSEMBL	ss133313243	Dec 01, 2009 (131)
18	ENSEMBL	ss139470046	Dec 01, 2009 (131)
19	ILLUMINA	ss152537325	Dec 01, 2009 (131)
20	GMI	ss156924035	Dec 01, 2009 (131)
21	ILLUMINA	ss159102806	Dec 01, 2009 (131)
22	ILLUMINA	ss159849738	Dec 01, 2009 (131)
23	COMPLETE_GENOMICS	ss161932853	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss163154677	Jul 04, 2010 (132)
25	COMPLETE_GENOMICS	ss166232071	Jul 04, 2010 (132)
26	ILLUMINA	ss169483688	Jul 04, 2010 (132)
27	BUSHMAN	ss198123791	Jul 04, 2010 (132)
28	BCM-HGSC-SUB	ss206269587	Jul 04, 2010 (132)
29	1000GENOMES	ss220770953	Jul 14, 2010 (132)
30	1000GENOMES	ss232280969	Jul 14, 2010 (132)
31	1000GENOMES	ss239597144	Jul 15, 2010 (132)
32	BL	ss252964659	May 09, 2011 (134)
33	GMI	ss277595315	May 04, 2012 (137)
34	GMI	ss284855829	Apr 25, 2013 (138)
35	PJP	ss293296430	May 09, 2011 (134)
36	ILLUMINA	ss479152948	May 04, 2012 (137)
37	ILLUMINA	ss479153652	May 04, 2012 (137)
38	ILLUMINA	ss479465619	Sep 08, 2015 (146)
39	ILLUMINA	ss484377065	May 04, 2012 (137)
40	ILLUMINA	ss536563743	Sep 08, 2015 (146)
41	TISHKOFF	ss557345151	Apr 25, 2013 (138)
42	SSMP	ss651109901	Apr 25, 2013 (138)
43	ILLUMINA	ss778719117	Sep 08, 2015 (146)
44	ILLUMINA	ss782634828	Sep 08, 2015 (146)
45	ILLUMINA	ss783604385	Sep 08, 2015 (146)
46	ILLUMINA	ss831884890	Sep 08, 2015 (146)
47	ILLUMINA	ss832615602	Jul 13, 2019 (153)
48	ILLUMINA	ss834178494	Sep 08, 2015 (146)
49	EVA-GONL	ss979821448	Aug 21, 2014 (142)
50	JMKIDD_LAB	ss1071315757	Aug 21, 2014 (142)
51	1000GENOMES	ss1308640759	Aug 21, 2014 (142)
52	HAMMER_LAB	ss1397368441	Sep 08, 2015 (146)
53	DDI	ss1429790997	Apr 01, 2015 (144)
54	EVA_GENOME_DK	ss1580437425	Apr 01, 2015 (144)
55	EVA_DECODE	ss1589310308	Apr 01, 2015 (144)
56	EVA_UK10K_ALSPAC	ss1609519736	Apr 01, 2015 (144)
57	EVA_UK10K_TWINSUK	ss1652513769	Apr 01, 2015 (144)
58	EVA_SVP	ss1712655308	Apr 01, 2015 (144)
59	ILLUMINA	ss1752509188	Sep 08, 2015 (146)
60	HAMMER_LAB	ss1801075146	Sep 08, 2015 (146)
61	WEILL_CORNELL_DGM	ss1923059041	Feb 12, 2016 (147)
62	GENOMED	ss1969671721	Jul 19, 2016 (147)
63	JJLAB	ss2022103589	Sep 14, 2016 (149)
64	USC_VALOUEV	ss2150214044	Dec 20, 2016 (150)
65	HUMAN_LONGEVITY	ss2260826924	Dec 20, 2016 (150)
66	SYSTEMSBIOZJU	ss2625552927	Nov 08, 2017 (151)
67	ILLUMINA	ss2634088500	Nov 08, 2017 (151)
68	GRF	ss2705659016	Nov 08, 2017 (151)
69	ILLUMINA	ss2710999966	Nov 08, 2017 (151)
70	GNOMAD	ss2806217991	Nov 08, 2017 (151)
71	SWEGEN	ss2994225894	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3024821106	Nov 08, 2017 (151)
73	CSHL	ss3345570553	Nov 08, 2017 (151)
74	ILLUMINA	ss3628912948	Oct 12, 2018 (152)
75	ILLUMINA	ss3632026839	Oct 12, 2018 (152)
76	ILLUMINA	ss3633327427	Oct 12, 2018 (152)
77	ILLUMINA	ss3634046166	Oct 12, 2018 (152)
78	ILLUMINA	ss3634943146	Oct 12, 2018 (152)
79	ILLUMINA	ss3635729264	Oct 12, 2018 (152)
80	ILLUMINA	ss3636644651	Oct 12, 2018 (152)
81	ILLUMINA	ss3637481761	Oct 12, 2018 (152)
82	ILLUMINA	ss3638474368	Oct 12, 2018 (152)
83	ILLUMINA	ss3639239818	Oct 12, 2018 (152)
84	ILLUMINA	ss3639919179	Oct 12, 2018 (152)
85	ILLUMINA	ss3640650442	Oct 12, 2018 (152)
86	ILLUMINA	ss3643426648	Oct 12, 2018 (152)
87	ILLUMINA	ss3643965555	Oct 12, 2018 (152)
88	URBANLAB	ss3647664433	Oct 12, 2018 (152)
89	EGCUT_WGS	ss3662134585	Jul 13, 2019 (153)
90	EVA_DECODE	ss3711509921	Jul 13, 2019 (153)
91	ACPOP	ss3730902763	Jul 13, 2019 (153)
92	ILLUMINA	ss3745243438	Jul 13, 2019 (153)
93	EVA	ss3761463869	Jul 13, 2019 (153)
94	ILLUMINA	ss3772738120	Jul 13, 2019 (153)
95	PACBIO	ss3784634176	Jul 13, 2019 (153)
96	PACBIO	ss3790102908	Jul 13, 2019 (153)
97	PACBIO	ss3794977980	Jul 13, 2019 (153)
98	KHV_HUMAN_GENOMES	ss3804596568	Jul 13, 2019 (153)
99	EVA	ss3828397189	Apr 26, 2020 (154)
100	EVA	ss3837632232	Apr 26, 2020 (154)
101	EVA	ss3843066485	Apr 26, 2020 (154)
102	HGDP	ss3847742713	Apr 26, 2020 (154)
103	SGDP_PRJ	ss3858333447	Apr 26, 2020 (154)
104	KRGDB	ss3904485101	Apr 26, 2020 (154)
105	KOGIC	ss3953629481	Apr 26, 2020 (154)
106	EVA	ss3985055724	Apr 26, 2021 (155)
107	EVA	ss4017134827	Apr 26, 2021 (155)
108	TOPMED	ss4604605797	Apr 26, 2021 (155)
109	TOMMO_GENOMICS	ss5164435657	Apr 26, 2021 (155)
110	1000G_HIGH_COVERAGE	ss5258228415	Oct 13, 2022 (156)
111	GENOGRAPHIC	ss5314497021	Oct 13, 2022 (156)
112	EVA	ss5314939563	Oct 13, 2022 (156)
113	EVA	ss5347239883	Oct 13, 2022 (156)
114	HUGCELL_USP	ss5457107982	Oct 13, 2022 (156)
115	1000G_HIGH_COVERAGE	ss5538757903	Oct 13, 2022 (156)
116	SANFORD_IMAGENETICS	ss5634455871	Oct 13, 2022 (156)
117	TOMMO_GENOMICS	ss5698149929	Oct 13, 2022 (156)
118	EVA	ss5799608797	Oct 13, 2022 (156)
119	YY_MCH	ss5804804747	Oct 13, 2022 (156)
120	EVA	ss5843623941	Oct 13, 2022 (156)
121	EVA	ss5854101788	Oct 13, 2022 (156)
122	EVA	ss5862354857	Oct 13, 2022 (156)
123	EVA	ss5962835113	Oct 13, 2022 (156)
124	EVA	ss5980210452	Oct 13, 2022 (156)
125	1000Genomes	NC_000004.11 - 17348363	Oct 12, 2018 (152)
126	1000Genomes_30x	NC_000004.12 - 17346740	Oct 13, 2022 (156)
127	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 17348363	Oct 12, 2018 (152)
128	Genome-wide autozygosity in Daghestan	NC_000004.10 - 16957461	Apr 26, 2020 (154)
129	Genetic variation in the Estonian population	NC_000004.11 - 17348363	Oct 12, 2018 (152)
130	Genographic Project	NC_000004.12 - 17346740	Oct 13, 2022 (156)
131	The Danish reference pan genome	NC_000004.11 - 17348363	Apr 26, 2020 (154)
132	gnomAD - Genomes	NC_000004.12 - 17346740	Apr 26, 2021 (155)
133	Genome of the Netherlands Release 5	NC_000004.11 - 17348363	Apr 26, 2020 (154)
134	HGDP-CEPH-db Supplement 1	NC_000004.10 - 16957461	Apr 26, 2020 (154)
135	HapMap	NC_000004.12 - 17346740	Apr 26, 2020 (154)
136	KOREAN population from KRGDB	NC_000004.11 - 17348363	Apr 26, 2020 (154)
137	Korean Genome Project	NC_000004.12 - 17346740	Apr 26, 2020 (154)
138	Northern Sweden	NC_000004.11 - 17348363	Jul 13, 2019 (153)
139	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 17348363	Apr 26, 2021 (155)
140	Qatari	NC_000004.11 - 17348363	Apr 26, 2020 (154)
141	SGDP_PRJ	NC_000004.11 - 17348363	Apr 26, 2020 (154)
142	Siberian	NC_000004.11 - 17348363	Apr 26, 2020 (154)
143	8.3KJPN	NC_000004.11 - 17348363	Apr 26, 2021 (155)
144	14KJPN	NC_000004.12 - 17346740	Oct 13, 2022 (156)
145	TopMed	NC_000004.12 - 17346740	Apr 26, 2021 (155)
146	UK 10K study - Twins	NC_000004.11 - 17348363	Oct 12, 2018 (152)
147	A Vietnamese Genetic Variation Database	NC_000004.11 - 17348363	Jul 13, 2019 (153)
148	ALFA	NC_000004.12 - 17346740	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)
rs57121662	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
11662495, ss3904485101	NC_000004.11:17348362:C:A	NC_000004.12:17346739:C:A	(self)
ss3639239818, ss3639919179, ss3643965555	NC_000004.9:17024631:C:T	NC_000004.12:17346739:C:T	(self)
344067, 420605, ss92488256, ss111864469, ss112959141, ss161932853, ss163154677, ss166232071, ss198123791, ss206269587, ss252964659, ss277595315, ss284855829, ss293296430, ss479152948, ss1397368441, ss1589310308, ss1712655308, ss3643426648, ss3847742713	NC_000004.10:16957460:C:T	NC_000004.12:17346739:C:T	(self)
19995455, 11136966, 7872833, 6602364, 4900980, 11662495, 4187628, 281651, 5100971, 10350427, 2730398, 22404964, 11136966, 2434109, ss220770953, ss232280969, ss239597144, ss479153652, ss479465619, ss484377065, ss536563743, ss557345151, ss651109901, ss778719117, ss782634828, ss783604385, ss831884890, ss832615602, ss834178494, ss979821448, ss1071315757, ss1308640759, ss1429790997, ss1580437425, ss1609519736, ss1652513769, ss1752509188, ss1801075146, ss1923059041, ss1969671721, ss2022103589, ss2150214044, ss2625552927, ss2634088500, ss2705659016, ss2710999966, ss2806217991, ss2994225894, ss3345570553, ss3628912948, ss3632026839, ss3633327427, ss3634046166, ss3634943146, ss3635729264, ss3636644651, ss3637481761, ss3638474368, ss3640650442, ss3662134585, ss3730902763, ss3745243438, ss3761463869, ss3772738120, ss3784634176, ss3790102908, ss3794977980, ss3828397189, ss3837632232, ss3858333447, ss3904485101, ss3985055724, ss4017134827, ss5164435657, ss5314939563, ss5347239883, ss5634455871, ss5799608797, ss5843623941, ss5962835113, ss5980210452	NC_000004.11:17348362:C:T	NC_000004.12:17346739:C:T	(self)
26283838, 49756, 141722822, 2566495, 10007482, 31987033, 441983353, 12537199842, ss2260826924, ss3024821106, ss3647664433, ss3711509921, ss3804596568, ss3843066485, ss3953629481, ss4604605797, ss5258228415, ss5314497021, ss5457107982, ss5538757903, ss5698149929, ss5804804747, ss5854101788, ss5862354857	NC_000004.12:17346739:C:T	NC_000004.12:17346739:C:T	(self)
ss13845725, ss19565940, ss20195305	NT_006316.15:8023720:C:T	NC_000004.12:17346739:C:T	(self)
ss23316471, ss44553534, ss66863605, ss66932304, ss68074909, ss70458953, ss70979495, ss75674072, ss84887359, ss104045395, ss133313243, ss139470046, ss152537325, ss156924035, ss159102806, ss159849738, ss169483688	NT_006316.16:8530159:C:T	NC_000004.12:17346739: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 rs10000081

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10000081