Name: rs10786068
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.

rs10786068

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:93082720 (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>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.286070 (75720/264690, TOPMED)
C=0.291377 (40805/140042, GnomAD)
C=0.28335 (22300/78700, PAGE_STUDY) (+ 18 more)
C=0.27826 (7863/28258, 14KJPN)
C=0.30148 (5695/18890, ALFA)
C=0.27667 (4637/16760, 8.3KJPN)
C=0.2483 (1590/6404, 1000G_30x)
C=0.2472 (1238/5008, 1000G)
C=0.3205 (1436/4480, Estonian)
C=0.3028 (1167/3854, ALSPAC)
C=0.3029 (1123/3708, TWINSUK)
C=0.2493 (730/2928, KOREAN)
C=0.2440 (447/1832, Korea1K)
C=0.271 (270/998, GoNL)
C=0.285 (171/600, NorthernSweden)
C=0.200 (104/520, SGDP_PRJ)
C=0.305 (100/328, HapMap)
C=0.241 (52/216, Qatari)
C=0.190 (40/210, Vietnamese)
C=0.20 (11/54, Siberian)
C=0.35 (14/40, 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	18890	C=0.30148	G=0.69852
European	Sub	14286	C=0.30512	G=0.69488
African	Sub	2946	C=0.2828	G=0.7172
African Others	Sub	114	C=0.289	G=0.711
African American	Sub	2832	C=0.2825	G=0.7175
Asian	Sub	112	C=0.152	G=0.848
East Asian	Sub	86	C=0.14	G=0.86
Other Asian	Sub	26	C=0.19	G=0.81
Latin American 1	Sub	146	C=0.247	G=0.753
Latin American 2	Sub	610	C=0.364	G=0.636
South Asian	Sub	98	C=0.21	G=0.79
Other	Sub	692	C=0.299	G=0.701

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=0.286070	G=0.713930
gnomAD - Genomes	Global	Study-wide	140042	C=0.291377	G=0.708623
gnomAD - Genomes	European	Sub	75844	C=0.30481	G=0.69519
gnomAD - Genomes	African	Sub	41954	C=0.28143	G=0.71857
gnomAD - Genomes	American	Sub	13640	C=0.29120	G=0.70880
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	C=0.2275	G=0.7725
gnomAD - Genomes	East Asian	Sub	3132	C=0.1782	G=0.8218
gnomAD - Genomes	Other	Sub	2154	C=0.2762	G=0.7238
The PAGE Study	Global	Study-wide	78700	C=0.28335	G=0.71665
The PAGE Study	AfricanAmerican	Sub	32516	C=0.27820	G=0.72180
The PAGE Study	Mexican	Sub	10810	C=0.33497	G=0.66503
The PAGE Study	Asian	Sub	8318	C=0.2532	G=0.7468
The PAGE Study	PuertoRican	Sub	7918	C=0.3050	G=0.6950
The PAGE Study	NativeHawaiian	Sub	4534	C=0.2131	G=0.7869
The PAGE Study	Cuban	Sub	4230	C=0.2792	G=0.7208
The PAGE Study	Dominican	Sub	3826	C=0.2739	G=0.7261
The PAGE Study	CentralAmerican	Sub	2450	C=0.2878	G=0.7122
The PAGE Study	SouthAmerican	Sub	1982	C=0.2977	G=0.7023
The PAGE Study	NativeAmerican	Sub	1260	C=0.3238	G=0.6762
The PAGE Study	SouthAsian	Sub	856	C=0.250	G=0.750
14KJPN	JAPANESE	Study-wide	28258	C=0.27826	G=0.72174
Allele Frequency Aggregator	Total	Global	18890	C=0.30148	G=0.69852
Allele Frequency Aggregator	European	Sub	14286	C=0.30512	G=0.69488
Allele Frequency Aggregator	African	Sub	2946	C=0.2828	G=0.7172
Allele Frequency Aggregator	Other	Sub	692	C=0.299	G=0.701
Allele Frequency Aggregator	Latin American 2	Sub	610	C=0.364	G=0.636
Allele Frequency Aggregator	Latin American 1	Sub	146	C=0.247	G=0.753
Allele Frequency Aggregator	Asian	Sub	112	C=0.152	G=0.848
Allele Frequency Aggregator	South Asian	Sub	98	C=0.21	G=0.79
8.3KJPN	JAPANESE	Study-wide	16760	C=0.27667	G=0.72333
1000Genomes_30x	Global	Study-wide	6404	C=0.2483	G=0.7517
1000Genomes_30x	African	Sub	1786	C=0.2587	G=0.7413
1000Genomes_30x	Europe	Sub	1266	C=0.2867	G=0.7133
1000Genomes_30x	South Asian	Sub	1202	C=0.2404	G=0.7596
1000Genomes_30x	East Asian	Sub	1170	C=0.1838	G=0.8162
1000Genomes_30x	American	Sub	980	C=0.266	G=0.734
1000Genomes	Global	Study-wide	5008	C=0.2472	G=0.7528
1000Genomes	African	Sub	1322	C=0.2610	G=0.7390
1000Genomes	East Asian	Sub	1008	C=0.1845	G=0.8155
1000Genomes	Europe	Sub	1006	C=0.2942	G=0.7058
1000Genomes	South Asian	Sub	978	C=0.231	G=0.769
1000Genomes	American	Sub	694	C=0.267	G=0.733
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.3205	G=0.6795
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.3028	G=0.6972
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.3029	G=0.6971
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.2493	G=0.7507
Korean Genome Project	KOREAN	Study-wide	1832	C=0.2440	G=0.7560
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.271	G=0.729
Northern Sweden	ACPOP	Study-wide	600	C=0.285	G=0.715
SGDP_PRJ	Global	Study-wide	520	C=0.200	G=0.800
HapMap	Global	Study-wide	328	C=0.305	G=0.695
HapMap	African	Sub	120	C=0.250	G=0.750
HapMap	American	Sub	120	C=0.333	G=0.667
HapMap	Asian	Sub	88	C=0.34	G=0.66
Qatari	Global	Study-wide	216	C=0.241	G=0.759
A Vietnamese Genetic Variation Database	Global	Study-wide	210	C=0.190	G=0.810
Siberian	Global	Study-wide	54	C=0.20	G=0.80
The Danish reference pan genome	Danish	Study-wide	40	C=0.35	G=0.65

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.93082720C>G
GRCh37.p13 chr 10	NC_000010.10:g.94842477C>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	C=	G
GRCh38.p14 chr 10	NC_000010.11:g.93082720=	NC_000010.11:g.93082720C>G
GRCh37.p13 chr 10	NC_000010.10:g.94842477=	NC_000010.10:g.94842477C>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#.

122 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss15879432	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss16483236	Feb 27, 2004 (120)
3	SC_SNP	ss18637664	Feb 27, 2004 (120)
4	SC_SNP	ss18881243	Feb 27, 2004 (120)
5	SSAHASNP	ss20703771	Apr 05, 2004 (121)
6	PERLEGEN	ss24545839	Sep 20, 2004 (123)
7	ABI	ss38634168	Mar 15, 2006 (126)
8	PERLEGEN	ss69087768	May 16, 2007 (127)
9	ILLUMINA	ss75243144	Dec 07, 2007 (129)
10	HGSV	ss77232951	Dec 07, 2007 (129)
11	HGSV	ss82205279	Dec 15, 2007 (130)
12	HUMANGENOME_JCVI	ss97674573	Feb 06, 2009 (130)
13	KRIBB_YJKIM	ss102648491	Feb 06, 2009 (130)
14	BGI	ss106694877	Feb 06, 2009 (130)
15	1000GENOMES	ss109658490	Jan 24, 2009 (130)
16	1000GENOMES	ss113656964	Jan 25, 2009 (130)
17	ILLUMINA-UK	ss119270517	Feb 15, 2009 (130)
18	ENSEMBL	ss131940340	Dec 01, 2009 (131)
19	GMI	ss155390613	Dec 01, 2009 (131)
20	ILLUMINA	ss159920349	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss168680177	Jul 04, 2010 (132)
22	ILLUMINA	ss170523297	Jul 04, 2010 (132)
23	COMPLETE_GENOMICS	ss170752329	Jul 04, 2010 (132)
24	COMPLETE_GENOMICS	ss174696342	Jul 04, 2010 (132)
25	BUSHMAN	ss201870108	Jul 04, 2010 (132)
26	BCM-HGSC-SUB	ss207041712	Jul 04, 2010 (132)
27	1000GENOMES	ss224877884	Jul 14, 2010 (132)
28	1000GENOMES	ss235287878	Jul 15, 2010 (132)
29	1000GENOMES	ss241972248	Jul 15, 2010 (132)
30	ILLUMINA	ss244270140	Jul 04, 2010 (132)
31	BL	ss254523382	May 09, 2011 (134)
32	GMI	ss280727977	May 04, 2012 (137)
33	GMI	ss286241621	Apr 25, 2013 (138)
34	PJP	ss290897004	May 09, 2011 (134)
35	ILLUMINA	ss479347755	May 04, 2012 (137)
36	ILLUMINA	ss479350974	May 04, 2012 (137)
37	ILLUMINA	ss479747419	Sep 08, 2015 (146)
38	ILLUMINA	ss484474117	May 04, 2012 (137)
39	ILLUMINA	ss536633967	Sep 08, 2015 (146)
40	TISHKOFF	ss562135572	Apr 25, 2013 (138)
41	SSMP	ss657171011	Apr 25, 2013 (138)
42	ILLUMINA	ss778342325	Aug 21, 2014 (142)
43	ILLUMINA	ss782683597	Aug 21, 2014 (142)
44	ILLUMINA	ss783652016	Aug 21, 2014 (142)
45	ILLUMINA	ss831934432	Apr 01, 2015 (144)
46	ILLUMINA	ss833796935	Aug 21, 2014 (142)
47	EVA-GONL	ss987791383	Aug 21, 2014 (142)
48	JMKIDD_LAB	ss1077206239	Aug 21, 2014 (142)
49	1000GENOMES	ss1338576483	Aug 21, 2014 (142)
50	DDI	ss1426407440	Apr 01, 2015 (144)
51	EVA_GENOME_DK	ss1575289959	Apr 01, 2015 (144)
52	EVA_DECODE	ss1597464664	Apr 01, 2015 (144)
53	EVA_UK10K_ALSPAC	ss1625170299	Apr 01, 2015 (144)
54	EVA_UK10K_TWINSUK	ss1668164332	Apr 01, 2015 (144)
55	ILLUMINA	ss1751987499	Sep 08, 2015 (146)
56	HAMMER_LAB	ss1806515751	Sep 08, 2015 (146)
57	WEILL_CORNELL_DGM	ss1931157806	Feb 12, 2016 (147)
58	ILLUMINA	ss1959283808	Feb 12, 2016 (147)
59	GENOMED	ss1967197253	Jul 19, 2016 (147)
60	JJLAB	ss2026307483	Sep 14, 2016 (149)
61	USC_VALOUEV	ss2154583579	Nov 08, 2017 (151)
62	HUMAN_LONGEVITY	ss2177052553	Dec 20, 2016 (150)
63	SYSTEMSBIOZJU	ss2627622441	Nov 08, 2017 (151)
64	ILLUMINA	ss2632746781	Nov 08, 2017 (151)
65	ILLUMINA	ss2635017925	Nov 08, 2017 (151)
66	GRF	ss2698835939	Nov 08, 2017 (151)
67	GNOMAD	ss2891997744	Nov 08, 2017 (151)
68	AFFY	ss2984919520	Nov 08, 2017 (151)
69	AFFY	ss2985568098	Nov 08, 2017 (151)
70	SWEGEN	ss3006946386	Nov 08, 2017 (151)
71	ILLUMINA	ss3021263706	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3026943506	Nov 08, 2017 (151)
73	CSHL	ss3349255974	Nov 08, 2017 (151)
74	ILLUMINA	ss3626507070	Oct 12, 2018 (152)
75	ILLUMINA	ss3630770144	Oct 12, 2018 (152)
76	ILLUMINA	ss3632959826	Oct 12, 2018 (152)
77	ILLUMINA	ss3633657453	Oct 12, 2018 (152)
78	ILLUMINA	ss3634417064	Oct 12, 2018 (152)
79	ILLUMINA	ss3635349739	Oct 12, 2018 (152)
80	ILLUMINA	ss3636100849	Oct 12, 2018 (152)
81	ILLUMINA	ss3637100443	Oct 12, 2018 (152)
82	ILLUMINA	ss3637866494	Oct 12, 2018 (152)
83	ILLUMINA	ss3640124405	Oct 12, 2018 (152)
84	ILLUMINA	ss3642868618	Oct 12, 2018 (152)
85	URBANLAB	ss3649438442	Oct 12, 2018 (152)
86	ILLUMINA	ss3651622080	Oct 12, 2018 (152)
87	ILLUMINA	ss3653690217	Oct 12, 2018 (152)
88	EGCUT_WGS	ss3674358500	Jul 13, 2019 (153)
89	EVA_DECODE	ss3690437851	Jul 13, 2019 (153)
90	ILLUMINA	ss3725178423	Jul 13, 2019 (153)
91	ACPOP	ss3737574858	Jul 13, 2019 (153)
92	ILLUMINA	ss3744718038	Jul 13, 2019 (153)
93	EVA	ss3748454173	Jul 13, 2019 (153)
94	PAGE_CC	ss3771574839	Jul 13, 2019 (153)
95	ILLUMINA	ss3772218401	Jul 13, 2019 (153)
96	PACBIO	ss3786753427	Jul 13, 2019 (153)
97	PACBIO	ss3791921337	Jul 13, 2019 (153)
98	PACBIO	ss3796803464	Jul 13, 2019 (153)
99	KHV_HUMAN_GENOMES	ss3813820305	Jul 13, 2019 (153)
100	EVA	ss3832270178	Apr 26, 2020 (154)
101	EVA	ss3839676233	Apr 26, 2020 (154)
102	EVA	ss3845149824	Apr 26, 2020 (154)
103	SGDP_PRJ	ss3874803898	Apr 26, 2020 (154)
104	KRGDB	ss3922929004	Apr 26, 2020 (154)
105	KOGIC	ss3968435620	Apr 26, 2020 (154)
106	EVA	ss4017500846	Apr 26, 2021 (155)
107	TOPMED	ss4862225868	Apr 26, 2021 (155)
108	TOMMO_GENOMICS	ss5198917540	Apr 26, 2021 (155)
109	1000G_HIGH_COVERAGE	ss5285047503	Oct 16, 2022 (156)
110	EVA	ss5315493590	Oct 16, 2022 (156)
111	EVA	ss5395250700	Oct 16, 2022 (156)
112	HUGCELL_USP	ss5480511108	Oct 16, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5579503823	Oct 16, 2022 (156)
114	SANFORD_IMAGENETICS	ss5649863052	Oct 16, 2022 (156)
115	TOMMO_GENOMICS	ss5745119367	Oct 16, 2022 (156)
116	EVA	ss5799821155	Oct 16, 2022 (156)
117	YY_MCH	ss5811782592	Oct 16, 2022 (156)
118	EVA	ss5824791821	Oct 16, 2022 (156)
119	EVA	ss5849692106	Oct 16, 2022 (156)
120	EVA	ss5880038419	Oct 16, 2022 (156)
121	EVA	ss5941147907	Oct 16, 2022 (156)
122	EVA	ss5980630470	Oct 16, 2022 (156)
123	1000Genomes	NC_000010.10 - 94842477	Oct 12, 2018 (152)
124	1000Genomes_30x	NC_000010.11 - 93082720	Oct 16, 2022 (156)
125	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 94842477	Oct 12, 2018 (152)
126	Genetic variation in the Estonian population	NC_000010.10 - 94842477	Oct 12, 2018 (152)
127	The Danish reference pan genome	NC_000010.10 - 94842477	Apr 26, 2020 (154)
128	gnomAD - Genomes	NC_000010.11 - 93082720	Apr 26, 2021 (155)
129	Genome of the Netherlands Release 5	NC_000010.10 - 94842477	Apr 26, 2020 (154)
130	HapMap	NC_000010.11 - 93082720	Apr 26, 2020 (154)
131	KOREAN population from KRGDB	NC_000010.10 - 94842477	Apr 26, 2020 (154)
132	Korean Genome Project	NC_000010.11 - 93082720	Apr 26, 2020 (154)
133	Northern Sweden	NC_000010.10 - 94842477	Jul 13, 2019 (153)
134	The PAGE Study	NC_000010.11 - 93082720	Jul 13, 2019 (153)
135	Qatari	NC_000010.10 - 94842477	Apr 26, 2020 (154)
136	SGDP_PRJ	NC_000010.10 - 94842477	Apr 26, 2020 (154)
137	Siberian	NC_000010.10 - 94842477	Apr 26, 2020 (154)
138	8.3KJPN	NC_000010.10 - 94842477	Apr 26, 2021 (155)
139	14KJPN	NC_000010.11 - 93082720	Oct 16, 2022 (156)
140	TopMed	NC_000010.11 - 93082720	Apr 26, 2021 (155)
141	UK 10K study - Twins	NC_000010.10 - 94842477	Oct 12, 2018 (152)
142	A Vietnamese Genetic Variation Database	NC_000010.10 - 94842477	Jul 13, 2019 (153)
143	ALFA	NC_000010.11 - 93082720	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)
rs17465801	Oct 08, 2004 (123)
rs60790253	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss77232951, ss82205279	NC_000010.8:94832466:C:G	NC_000010.11:93082719:C:G	(self)
ss109658490, ss113656964, ss119270517, ss168680177, ss170752329, ss174696342, ss201870108, ss207041712, ss254523382, ss280727977, ss286241621, ss290897004, ss479347755, ss1597464664, ss2635017925, ss3642868618	NC_000010.9:94832466:C:G	NC_000010.11:93082719:C:G	(self)
51006185, 28317158, 20096748, 2277971, 12626518, 30106398, 10859723, 13199736, 26820878, 7099933, 56886847, 28317158, 6288389, ss224877884, ss235287878, ss241972248, ss479350974, ss479747419, ss484474117, ss536633967, ss562135572, ss657171011, ss778342325, ss782683597, ss783652016, ss831934432, ss833796935, ss987791383, ss1077206239, ss1338576483, ss1426407440, ss1575289959, ss1625170299, ss1668164332, ss1751987499, ss1806515751, ss1931157806, ss1959283808, ss1967197253, ss2026307483, ss2154583579, ss2627622441, ss2632746781, ss2698835939, ss2891997744, ss2984919520, ss2985568098, ss3006946386, ss3021263706, ss3349255974, ss3626507070, ss3630770144, ss3632959826, ss3633657453, ss3634417064, ss3635349739, ss3636100849, ss3637100443, ss3637866494, ss3640124405, ss3651622080, ss3653690217, ss3674358500, ss3737574858, ss3744718038, ss3748454173, ss3772218401, ss3786753427, ss3791921337, ss3796803464, ss3832270178, ss3839676233, ss3874803898, ss3922929004, ss4017500846, ss5198917540, ss5315493590, ss5395250700, ss5649863052, ss5799821155, ss5824791821, ss5941147907, ss5980630470	NC_000010.10:94842476:C:G	NC_000010.11:93082719:C:G	(self)
67029758, 360400320, 465728, 24813621, 796308, 78956471, 77771523, 6082731331, ss2177052553, ss3026943506, ss3649438442, ss3690437851, ss3725178423, ss3771574839, ss3813820305, ss3845149824, ss3968435620, ss4862225868, ss5285047503, ss5480511108, ss5579503823, ss5745119367, ss5811782592, ss5849692106, ss5880038419	NC_000010.11:93082719:C:G	NC_000010.11:93082719:C:G	(self)
ss15879432, ss16483236, ss18637664, ss18881243, ss20703771	NT_030059.11:13591002:C:G	NC_000010.11:93082719:C:G	(self)
ss24545839, ss38634168, ss69087768, ss75243144, ss97674573, ss102648491, ss106694877, ss131940340, ss155390613, ss159920349, ss170523297, ss244270140	NT_030059.13:45646940:C:G	NC_000010.11:93082719:C: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 rs10786068

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

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