Name: rs10904561
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.

rs10904561

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:89716 (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: T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.255435 (67611/264690, TOPMED)
G=0.321846 (68642/213276, ALFA)
G=0.269575 (37726/139946, GnomAD) (+ 21 more)
G=0.12612 (3564/28258, 14KJPN)
G=0.12816 (2148/16760, 8.3KJPN)
G=0.2400 (1537/6404, 1000G_30x)
G=0.2430 (1217/5008, 1000G)
G=0.3574 (1601/4480, Estonian)
G=0.3264 (1258/3854, ALSPAC)
G=0.3239 (1201/3708, TWINSUK)
G=0.1884 (552/2930, KOREAN)
G=0.2675 (557/2082, HGDP_Stanford)
G=0.2183 (413/1892, HapMap)
G=0.2052 (376/1832, Korea1K)
G=0.327 (326/998, GoNL)
G=0.254 (200/786, PRJEB37584)
G=0.358 (215/600, NorthernSweden)
G=0.338 (73/216, Qatari)
G=0.266 (57/214, Vietnamese)
T=0.397 (81/204, SGDP_PRJ)
G=0.23 (9/40, GENOME_DK)
T=0.50 (12/24, Ancient Sardinia)
G=0.50 (12/24, Ancient Sardinia)
T=0.42 (10/24, Siberian)

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	218308	T=0.679164	G=0.320836
European	Sub	193082	T=0.665914	G=0.334086
African	Sub	7382	T=0.8460	G=0.1540
African Others	Sub	270	T=0.859	G=0.141
African American	Sub	7112	T=0.8455	G=0.1545
Asian	Sub	3644	T=0.8260	G=0.1740
East Asian	Sub	2980	T=0.8242	G=0.1758
Other Asian	Sub	664	T=0.834	G=0.166
Latin American 1	Sub	570	T=0.663	G=0.337
Latin American 2	Sub	5310	T=0.8004	G=0.1996
South Asian	Sub	324	T=0.682	G=0.318
Other	Sub	7996	T=0.6987	G=0.3013

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	T=0.744565	G=0.255435
Allele Frequency Aggregator	Total	Global	213276	T=0.678154	G=0.321846
Allele Frequency Aggregator	European	Sub	189992	T=0.665854	G=0.334146
Allele Frequency Aggregator	Other	Sub	7196	T=0.6929	G=0.3071
Allele Frequency Aggregator	African	Sub	6240	T=0.8465	G=0.1535
Allele Frequency Aggregator	Latin American 2	Sub	5310	T=0.8004	G=0.1996
Allele Frequency Aggregator	Asian	Sub	3644	T=0.8260	G=0.1740
Allele Frequency Aggregator	Latin American 1	Sub	570	T=0.663	G=0.337
Allele Frequency Aggregator	South Asian	Sub	324	T=0.682	G=0.318
gnomAD - Genomes	Global	Study-wide	139946	T=0.730425	G=0.269575
gnomAD - Genomes	European	Sub	75782	T=0.66476	G=0.33524
gnomAD - Genomes	African	Sub	41964	T=0.84270	G=0.15730
gnomAD - Genomes	American	Sub	13606	T=0.76033	G=0.23967
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	T=0.6742	G=0.3258
gnomAD - Genomes	East Asian	Sub	3124	T=0.7490	G=0.2510
gnomAD - Genomes	Other	Sub	2152	T=0.7240	G=0.2760
14KJPN	JAPANESE	Study-wide	28258	T=0.87388	G=0.12612
8.3KJPN	JAPANESE	Study-wide	16760	T=0.87184	G=0.12816
1000Genomes_30x	Global	Study-wide	6404	T=0.7600	G=0.2400
1000Genomes_30x	African	Sub	1786	T=0.8651	G=0.1349
1000Genomes_30x	Europe	Sub	1266	T=0.6445	G=0.3555
1000Genomes_30x	South Asian	Sub	1202	T=0.6814	G=0.3186
1000Genomes_30x	East Asian	Sub	1170	T=0.7658	G=0.2342
1000Genomes_30x	American	Sub	980	T=0.807	G=0.193
1000Genomes	Global	Study-wide	5008	T=0.7570	G=0.2430
1000Genomes	African	Sub	1322	T=0.8669	G=0.1331
1000Genomes	East Asian	Sub	1008	T=0.7679	G=0.2321
1000Genomes	Europe	Sub	1006	T=0.6481	G=0.3519
1000Genomes	South Asian	Sub	978	T=0.676	G=0.324
1000Genomes	American	Sub	694	T=0.804	G=0.196
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6426	G=0.3574
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6736	G=0.3264
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6761	G=0.3239
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.8116	G=0.1884
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	T=0.7325	G=0.2675
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.743	G=0.257
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.611	G=0.389
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.614	G=0.386
HGDP-CEPH-db Supplement 1	Europe	Sub	318	T=0.676	G=0.324
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.901	G=0.099
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.944	G=0.056
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.99	G=0.01
HapMap	Global	Study-wide	1892	T=0.7817	G=0.2183
HapMap	American	Sub	770	T=0.731	G=0.269
HapMap	African	Sub	692	T=0.838	G=0.162
HapMap	Asian	Sub	254	T=0.858	G=0.142
HapMap	Europe	Sub	176	T=0.670	G=0.330
Korean Genome Project	KOREAN	Study-wide	1832	T=0.7948	G=0.2052
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.673	G=0.327
CNV burdens in cranial meningiomas	Global	Study-wide	786	T=0.746	G=0.254
CNV burdens in cranial meningiomas	CRM	Sub	786	T=0.746	G=0.254
Northern Sweden	ACPOP	Study-wide	600	T=0.642	G=0.358
Qatari	Global	Study-wide	216	T=0.662	G=0.338
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.734	G=0.266
SGDP_PRJ	Global	Study-wide	204	T=0.397	G=0.603
The Danish reference pan genome	Danish	Study-wide	40	T=0.78	G=0.23
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	24	T=0.50	G=0.50
Siberian	Global	Study-wide	24	T=0.42	G=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 10	NC_000010.11:g.89716T>G
GRCh37.p13 chr 10	NC_000010.10:g.135656T>G
GRCh37.p13 chr 10 fix patch HG905_PATCH	NW_003571043.1:g.79716T>G

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	T=	G
GRCh38.p14 chr 10	NC_000010.11:g.89716=	NC_000010.11:g.89716T>G
GRCh37.p13 chr 10	NC_000010.10:g.135656=	NC_000010.10:g.135656T>G
GRCh37.p13 chr 10 fix patch HG905_PATCH	NW_003571043.1:g.79716=	NW_003571043.1:g.79716T>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#.

110 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss15977205	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss17395833	Feb 27, 2004 (120)
3	SC_SNP	ss18885663	Feb 27, 2004 (120)
4	ABI	ss39793227	Mar 14, 2006 (126)
5	ILLUMINA	ss67038475	Dec 01, 2006 (127)
6	PERLEGEN	ss69066476	May 18, 2007 (127)
7	ILLUMINA	ss71033408	May 18, 2007 (127)
8	ILLUMINA	ss75409485	Dec 06, 2007 (129)
9	HUMANGENOME_JCVI	ss97613060	Feb 04, 2009 (130)
10	BGI	ss102844558	Dec 01, 2009 (131)
11	KRIBB_YJKIM	ss119649569	Dec 01, 2009 (131)
12	ENSEMBL	ss138779858	Dec 01, 2009 (131)
13	ILLUMINA	ss159936620	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss167614018	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss170210104	Jul 04, 2010 (132)
16	ILLUMINA	ss170731865	Jul 04, 2010 (132)
17	BCM-HGSC-SUB	ss207281106	Jul 04, 2010 (132)
18	1000GENOMES	ss224512394	Jul 14, 2010 (132)
19	1000GENOMES	ss235012285	Jul 15, 2010 (132)
20	1000GENOMES	ss241753236	Jul 15, 2010 (132)
21	GMI	ss280440400	May 04, 2012 (137)
22	GMI	ss286110763	Apr 25, 2013 (138)
23	PJP	ss290815808	May 09, 2011 (134)
24	ILLUMINA	ss479398378	May 04, 2012 (137)
25	ILLUMINA	ss479401652	May 04, 2012 (137)
26	ILLUMINA	ss479812518	Sep 11, 2015 (146)
27	ILLUMINA	ss484499190	May 04, 2012 (137)
28	ILLUMINA	ss536651284	Sep 11, 2015 (146)
29	TISHKOFF	ss561707942	Apr 25, 2013 (138)
30	SSMP	ss656208288	Apr 25, 2013 (138)
31	ILLUMINA	ss778370041	Sep 11, 2015 (146)
32	ILLUMINA	ss782696138	Sep 11, 2015 (146)
33	ILLUMINA	ss783664276	Sep 11, 2015 (146)
34	ILLUMINA	ss831947187	Sep 11, 2015 (146)
35	ILLUMINA	ss833824905	Sep 11, 2015 (146)
36	EVA-GONL	ss987096795	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1076687425	Aug 21, 2014 (142)
38	1000GENOMES	ss1335912983	Aug 21, 2014 (142)
39	DDI	ss1426189111	Apr 09, 2015 (144)
40	EVA_GENOME_DK	ss1574842108	Apr 09, 2015 (144)
41	EVA_UK10K_ALSPAC	ss1623797627	Apr 09, 2015 (144)
42	EVA_UK10K_TWINSUK	ss1666791660	Apr 09, 2015 (144)
43	EVA_SVP	ss1713149053	Apr 01, 2015 (144)
44	ILLUMINA	ss1751957838	Sep 11, 2015 (146)
45	WEILL_CORNELL_DGM	ss1930414780	Feb 17, 2016 (147)
46	ILLUMINA	ss1946273718	Feb 17, 2016 (147)
47	ILLUMINA	ss1959231575	Feb 17, 2016 (147)
48	JJLAB	ss2025929581	Sep 28, 2016 (149)
49	USC_VALOUEV	ss2154169641	Oct 12, 2018 (152)
50	HUMAN_LONGEVITY	ss2171932848	Dec 20, 2016 (150)
51	SYSTEMSBIOZJU	ss2627432630	Oct 12, 2018 (152)
52	ILLUMINA	ss2632661393	Oct 12, 2018 (152)
53	GRF	ss2698389039	Oct 12, 2018 (152)
54	ILLUMINA	ss2710700316	Oct 12, 2018 (152)
55	GNOMAD	ss2884519412	Oct 12, 2018 (152)
56	SWEGEN	ss3005784454	Oct 12, 2018 (152)
57	ILLUMINA	ss3021205017	Oct 12, 2018 (152)
58	BIOINF_KMB_FNS_UNIBA	ss3026746716	Nov 08, 2017 (151)
59	CSHL	ss3348911630	Oct 12, 2018 (152)
60	ILLUMINA	ss3625571647	Oct 12, 2018 (152)
61	ILLUMINA	ss3626364340	Oct 12, 2018 (152)
62	ILLUMINA	ss3630689705	Oct 12, 2018 (152)
63	ILLUMINA	ss3632934513	Oct 12, 2018 (152)
64	ILLUMINA	ss3633630986	Oct 12, 2018 (152)
65	ILLUMINA	ss3634385348	Oct 12, 2018 (152)
66	ILLUMINA	ss3635323875	Oct 12, 2018 (152)
67	ILLUMINA	ss3636064879	Oct 12, 2018 (152)
68	ILLUMINA	ss3637074442	Oct 12, 2018 (152)
69	ILLUMINA	ss3637828200	Oct 12, 2018 (152)
70	ILLUMINA	ss3640092696	Oct 12, 2018 (152)
71	ILLUMINA	ss3642833511	Oct 12, 2018 (152)
72	ILLUMINA	ss3644526390	Oct 12, 2018 (152)
73	URBANLAB	ss3649265508	Oct 12, 2018 (152)
74	ILLUMINA	ss3651551868	Oct 12, 2018 (152)
75	EGCUT_WGS	ss3673314809	Jul 13, 2019 (153)
76	EVA_DECODE	ss3689095376	Jul 13, 2019 (153)
77	ILLUMINA	ss3725127341	Jul 13, 2019 (153)
78	ACPOP	ss3736974333	Jul 13, 2019 (153)
79	ILLUMINA	ss3744064587	Jul 13, 2019 (153)
80	ILLUMINA	ss3744686239	Jul 13, 2019 (153)
81	EVA	ss3747627378	Jul 13, 2019 (153)
82	ILLUMINA	ss3772186965	Jul 13, 2019 (153)
83	KHV_HUMAN_GENOMES	ss3812993361	Jul 13, 2019 (153)
84	EVA	ss3831916755	Apr 26, 2020 (154)
85	HGDP	ss3847371751	Apr 26, 2020 (154)
86	SGDP_PRJ	ss3873326493	Apr 26, 2020 (154)
87	KRGDB	ss3921253527	Apr 26, 2020 (154)
88	KOGIC	ss3967022909	Apr 26, 2020 (154)
89	EVA	ss3984628064	Apr 26, 2021 (155)
90	EVA	ss3985451430	Apr 26, 2021 (155)
91	EVA	ss4017465204	Apr 26, 2021 (155)
92	GNOMAD	ss4211411244	Apr 26, 2021 (155)
93	TOPMED	ss4839524457	Apr 26, 2021 (155)
94	TOMMO_GENOMICS	ss5195848183	Apr 26, 2021 (155)
95	EVA	ss5237469539	Apr 26, 2021 (155)
96	1000G_HIGH_COVERAGE	ss5282596218	Oct 16, 2022 (156)
97	EVA	ss5315442459	Oct 16, 2022 (156)
98	HUGCELL_USP	ss5478409211	Oct 16, 2022 (156)
99	EVA	ss5509874339	Oct 16, 2022 (156)
100	1000G_HIGH_COVERAGE	ss5575841432	Oct 16, 2022 (156)
101	SANFORD_IMAGENETICS	ss5624236914	Oct 16, 2022 (156)
102	SANFORD_IMAGENETICS	ss5648489458	Oct 16, 2022 (156)
103	TOMMO_GENOMICS	ss5740573085	Oct 16, 2022 (156)
104	EVA	ss5799800033	Oct 16, 2022 (156)
105	YY_MCH	ss5811109603	Oct 16, 2022 (156)
106	EVA	ss5823842418	Oct 16, 2022 (156)
107	EVA	ss5849394441	Oct 16, 2022 (156)
108	EVA	ss5877372254	Oct 16, 2022 (156)
109	EVA	ss5939768863	Oct 16, 2022 (156)
110	EVA	ss5979313385	Oct 16, 2022 (156)
111	1000Genomes	NC_000010.10 - 135656	Oct 12, 2018 (152)
112	1000Genomes_30x	NC_000010.11 - 89716	Oct 16, 2022 (156)
113	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 135656	Oct 12, 2018 (152)
114	Genetic variation in the Estonian population	NC_000010.10 - 135656	Oct 12, 2018 (152)
115	The Danish reference pan genome	NC_000010.10 - 135656	Apr 26, 2020 (154)
116	gnomAD - Genomes	NC_000010.11 - 89716	Apr 26, 2021 (155)
117	Genome of the Netherlands Release 5	NC_000010.10 - 135656	Apr 26, 2020 (154)
118	HGDP-CEPH-db Supplement 1	NC_000010.9 - 125656	Apr 26, 2020 (154)
119	HapMap	NC_000010.11 - 89716	Apr 26, 2020 (154)
120	KOREAN population from KRGDB	NC_000010.10 - 135656	Apr 26, 2020 (154)
121	Korean Genome Project	NC_000010.11 - 89716	Apr 26, 2020 (154)
122	Northern Sweden	NC_000010.10 - 135656	Jul 13, 2019 (153)
123	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000010.10 - 135656	Apr 26, 2021 (155)
124	CNV burdens in cranial meningiomas	NC_000010.10 - 135656	Apr 26, 2021 (155)
125	Qatari	NC_000010.10 - 135656	Apr 26, 2020 (154)
126	SGDP_PRJ	NC_000010.10 - 135656	Apr 26, 2020 (154)
127	Siberian	NC_000010.10 - 135656	Apr 26, 2020 (154)
128	8.3KJPN	NC_000010.10 - 135656	Apr 26, 2021 (155)
129	14KJPN	NC_000010.11 - 89716	Oct 16, 2022 (156)
130	TopMed	NC_000010.11 - 89716	Apr 26, 2021 (155)
131	UK 10K study - Twins	NC_000010.10 - 135656	Oct 12, 2018 (152)
132	A Vietnamese Genetic Variation Database	NC_000010.10 - 135656	Jul 13, 2019 (153)
133	ALFA	NC_000010.11 - 89716	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)
rs56599187	May 24, 2008 (130)
rs386515850	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
49643, ss167614018, ss170210104, ss207281106, ss280440400, ss286110763, ss290815808, ss479398378, ss1713149053, ss3642833511, ss3847371751	NC_000010.9:125655:T:G	NC_000010.11:89715:T:G	(self)
48246693, 26806413, 19053057, 1988121, 11953922, 28430921, 10259198, 677357, 177519, 12456710, 25343473, 6685995, 53817490, 26806413, 5948678, ss224512394, ss235012285, ss241753236, ss479401652, ss479812518, ss484499190, ss536651284, ss561707942, ss656208288, ss778370041, ss782696138, ss783664276, ss831947187, ss833824905, ss987096795, ss1076687425, ss1335912983, ss1426189111, ss1574842108, ss1623797627, ss1666791660, ss1751957838, ss1930414780, ss1946273718, ss1959231575, ss2025929581, ss2154169641, ss2627432630, ss2632661393, ss2698389039, ss2710700316, ss2884519412, ss3005784454, ss3021205017, ss3348911630, ss3625571647, ss3626364340, ss3630689705, ss3632934513, ss3633630986, ss3634385348, ss3635323875, ss3636064879, ss3637074442, ss3637828200, ss3640092696, ss3644526390, ss3651551868, ss3673314809, ss3736974333, ss3744064587, ss3744686239, ss3747627378, ss3772186965, ss3831916755, ss3873326493, ss3921253527, ss3984628064, ss3985451430, ss4017465204, ss5195848183, ss5237469539, ss5315442459, ss5509874339, ss5624236914, ss5648489458, ss5799800033, ss5823842418, ss5939768863, ss5979313385	NC_000010.10:135655:T:G	NC_000010.11:89715:T:G	(self)
63367367, 340934431, 317110, 23400910, 74410189, 55070112, 5189037696, ss2171932848, ss3026746716, ss3649265508, ss3689095376, ss3725127341, ss3812993361, ss3967022909, ss4211411244, ss4839524457, ss5282596218, ss5478409211, ss5575841432, ss5740573085, ss5811109603, ss5849394441, ss5877372254	NC_000010.11:89715:T:G	NC_000010.11:89715:T:G	(self)
ss39793227, ss67038475, ss69066476, ss71033408, ss75409485, ss97613060, ss102844558, ss119649569, ss138779858, ss159936620, ss170731865	NT_008705.16:75655:T:G	NC_000010.11:89715:T:G	(self)
ss15977205, ss17395833, ss18885663	NT_077567.3:75655:T:G	NC_000010.11:89715:T: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 rs10904561

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

rs10904561