Name: rs8085804
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.

rs8085804

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:42708328 (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>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.495636 (131190/264690, TOPMED)
T=0.326929 (75384/230582, ALFA)
T=0.465517 (65138/139926, GnomAD) (+ 21 more)
C=0.35105 (27627/78698, PAGE_STUDY)
C=0.24290 (6864/28258, 14KJPN)
C=0.24296 (4072/16760, 8.3KJPN)
C=0.4151 (2658/6404, 1000G_30x)
C=0.4189 (2098/5008, 1000G)
T=0.2855 (1279/4480, Estonian)
T=0.2867 (1105/3854, ALSPAC)
T=0.2789 (1034/3708, TWINSUK)
C=0.2305 (675/2928, KOREAN)
C=0.4280 (892/2084, HGDP_Stanford)
C=0.3578 (677/1892, HapMap)
C=0.2118 (388/1832, Korea1K)
T=0.299 (298/998, GoNL)
C=0.246 (192/782, PRJEB37584)
T=0.282 (169/600, NorthernSweden)
C=0.248 (107/432, SGDP_PRJ)
T=0.472 (102/216, Qatari)
C=0.264 (56/212, Vietnamese)
T=0.29 (20/70, Ancient Sardinia)
T=0.23 (9/40, GENOME_DK)
C=0.45 (17/38, 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	230798	C=0.673099	T=0.326901
European	Sub	197856	C=0.715536	T=0.284464
African	Sub	8146	C=0.2367	T=0.7633
African Others	Sub	308	C=0.162	T=0.838
African American	Sub	7838	C=0.2396	T=0.7604
Asian	Sub	6368	C=0.2247	T=0.7753
East Asian	Sub	4534	C=0.2296	T=0.7704
Other Asian	Sub	1834	C=0.2126	T=0.7874
Latin American 1	Sub	550	C=0.524	T=0.476
Latin American 2	Sub	1572	C=0.4809	T=0.5191
South Asian	Sub	5138	C=0.6166	T=0.3834
Other	Sub	11168	C=0.55569	T=0.44431

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=0.504364	T=0.495636
Allele Frequency Aggregator	Total	Global	230582	C=0.673071	T=0.326929
Allele Frequency Aggregator	European	Sub	197676	C=0.715509	T=0.284491
Allele Frequency Aggregator	Other	Sub	11146	C=0.55545	T=0.44455
Allele Frequency Aggregator	African	Sub	8132	C=0.2367	T=0.7633
Allele Frequency Aggregator	Asian	Sub	6368	C=0.2247	T=0.7753
Allele Frequency Aggregator	South Asian	Sub	5138	C=0.6166	T=0.3834
Allele Frequency Aggregator	Latin American 2	Sub	1572	C=0.4809	T=0.5191
Allele Frequency Aggregator	Latin American 1	Sub	550	C=0.524	T=0.476
gnomAD - Genomes	Global	Study-wide	139926	C=0.534483	T=0.465517
gnomAD - Genomes	European	Sub	75812	C=0.71166	T=0.28834
gnomAD - Genomes	African	Sub	41950	C=0.23316	T=0.76684
gnomAD - Genomes	American	Sub	13606	C=0.49147	T=0.50853
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	C=0.7378	T=0.2622
gnomAD - Genomes	East Asian	Sub	3088	C=0.2422	T=0.7578
gnomAD - Genomes	Other	Sub	2152	C=0.5446	T=0.4554
The PAGE Study	Global	Study-wide	78698	C=0.35105	T=0.64895
The PAGE Study	AfricanAmerican	Sub	32514	C=0.24903	T=0.75097
The PAGE Study	Mexican	Sub	10808	C=0.48001	T=0.51999
The PAGE Study	Asian	Sub	8318	C=0.2560	T=0.7440
The PAGE Study	PuertoRican	Sub	7918	C=0.4855	T=0.5145
The PAGE Study	NativeHawaiian	Sub	4534	C=0.2786	T=0.7214
The PAGE Study	Cuban	Sub	4230	C=0.5730	T=0.4270
The PAGE Study	Dominican	Sub	3828	C=0.4297	T=0.5703
The PAGE Study	CentralAmerican	Sub	2450	C=0.4122	T=0.5878
The PAGE Study	SouthAmerican	Sub	1982	C=0.4213	T=0.5787
The PAGE Study	NativeAmerican	Sub	1260	C=0.5421	T=0.4579
The PAGE Study	SouthAsian	Sub	856	C=0.595	T=0.405
14KJPN	JAPANESE	Study-wide	28258	C=0.24290	T=0.75710
8.3KJPN	JAPANESE	Study-wide	16760	C=0.24296	T=0.75704
1000Genomes_30x	Global	Study-wide	6404	C=0.4151	T=0.5849
1000Genomes_30x	African	Sub	1786	C=0.1540	T=0.8460
1000Genomes_30x	Europe	Sub	1266	C=0.6959	T=0.3041
1000Genomes_30x	South Asian	Sub	1202	C=0.6231	T=0.3769
1000Genomes_30x	East Asian	Sub	1170	C=0.2658	T=0.7342
1000Genomes_30x	American	Sub	980	C=0.451	T=0.549
1000Genomes	Global	Study-wide	5008	C=0.4189	T=0.5811
1000Genomes	African	Sub	1322	C=0.1566	T=0.8434
1000Genomes	East Asian	Sub	1008	C=0.2679	T=0.7321
1000Genomes	Europe	Sub	1006	C=0.6958	T=0.3042
1000Genomes	South Asian	Sub	978	C=0.619	T=0.381
1000Genomes	American	Sub	694	C=0.455	T=0.545
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.7145	T=0.2855
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.7133	T=0.2867
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.7211	T=0.2789
KOREAN population from KRGDB	KOREAN	Study-wide	2928	C=0.2305	A=0.0000, G=0.0000, T=0.7695
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.4280	T=0.5720
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.270	T=0.730
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.585	T=0.415
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.563	T=0.437
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.700	T=0.300
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.190	T=0.810
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.245	T=0.755
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.04	T=0.96
HapMap	Global	Study-wide	1892	C=0.3578	T=0.6422
HapMap	American	Sub	770	C=0.501	T=0.499
HapMap	African	Sub	692	C=0.156	T=0.844
HapMap	Asian	Sub	254	C=0.232	T=0.768
HapMap	Europe	Sub	176	C=0.705	T=0.295
Korean Genome Project	KOREAN	Study-wide	1832	C=0.2118	T=0.7882
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.701	T=0.299
CNV burdens in cranial meningiomas	Global	Study-wide	782	C=0.246	T=0.754
CNV burdens in cranial meningiomas	CRM	Sub	782	C=0.246	T=0.754
Northern Sweden	ACPOP	Study-wide	600	C=0.718	T=0.282
SGDP_PRJ	Global	Study-wide	432	C=0.248	T=0.752
Qatari	Global	Study-wide	216	C=0.528	T=0.472
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.264	T=0.736
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	70	C=0.71	T=0.29
The Danish reference pan genome	Danish	Study-wide	40	C=0.78	T=0.23
Siberian	Global	Study-wide	38	C=0.45	T=0.55

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 18	NC_000018.10:g.42708328C>A
GRCh38.p14 chr 18	NC_000018.10:g.42708328C>G
GRCh38.p14 chr 18	NC_000018.10:g.42708328C>T
GRCh37.p13 chr 18	NC_000018.9:g.40288293C>A
GRCh37.p13 chr 18	NC_000018.9:g.40288293C>G
GRCh37.p13 chr 18	NC_000018.9:g.40288293C>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	G	T
GRCh38.p14 chr 18	NC_000018.10:g.42708328=	NC_000018.10:g.42708328C>A	NC_000018.10:g.42708328C>G	NC_000018.10:g.42708328C>T
GRCh37.p13 chr 18	NC_000018.9:g.40288293=	NC_000018.9:g.40288293C>A	NC_000018.9:g.40288293C>G	NC_000018.9:g.40288293C>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#.

114 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss12422392	Jul 11, 2003 (116)
2	ILLUMINA	ss66726106	Dec 03, 2006 (127)
3	ILLUMINA	ss67869988	Dec 03, 2006 (127)
4	ILLUMINA	ss68015439	Dec 03, 2006 (127)
5	ILLUMINA	ss70969615	May 25, 2008 (130)
6	ILLUMINA	ss71580061	May 16, 2007 (127)
7	ILLUMINA	ss75639092	Dec 07, 2007 (129)
8	ILLUMINA	ss79280942	Dec 15, 2007 (130)
9	KRIBB_YJKIM	ss84783753	Dec 15, 2007 (130)
10	BGI	ss103391278	Dec 01, 2009 (131)
11	1000GENOMES	ss110439433	Jan 24, 2009 (130)
12	1000GENOMES	ss114319033	Jan 25, 2009 (130)
13	ILLUMINA-UK	ss117855101	Feb 14, 2009 (130)
14	ILLUMINA	ss122899618	Dec 01, 2009 (131)
15	ILLUMINA	ss154468224	Dec 01, 2009 (131)
16	GMI	ss155096289	Dec 01, 2009 (131)
17	ILLUMINA	ss159642743	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss169650687	Jul 04, 2010 (132)
19	COMPLETE_GENOMICS	ss171737136	Jul 04, 2010 (132)
20	ILLUMINA	ss172396204	Jul 04, 2010 (132)
21	ILLUMINA	ss174712757	Jul 04, 2010 (132)
22	BUSHMAN	ss203205873	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss208109971	Jul 04, 2010 (132)
24	1000GENOMES	ss227839046	Jul 14, 2010 (132)
25	1000GENOMES	ss237450430	Jul 15, 2010 (132)
26	1000GENOMES	ss243703104	Jul 15, 2010 (132)
27	GMI	ss282975789	May 04, 2012 (137)
28	GMI	ss287276355	Apr 25, 2013 (138)
29	PJP	ss292163065	May 09, 2011 (134)
30	EXOME_CHIP	ss491532919	May 04, 2012 (137)
31	ILLUMINA	ss537554010	Sep 08, 2015 (146)
32	TISHKOFF	ss565617912	Apr 25, 2013 (138)
33	SSMP	ss661447816	Apr 25, 2013 (138)
34	ILLUMINA	ss780687029	Sep 08, 2015 (146)
35	ILLUMINA	ss783360572	Sep 08, 2015 (146)
36	ILLUMINA	ss825611460	Apr 01, 2015 (144)
37	ILLUMINA	ss833153589	Jul 13, 2019 (153)
38	EVA-GONL	ss993688328	Aug 21, 2014 (142)
39	JMKIDD_LAB	ss1081471377	Aug 21, 2014 (142)
40	1000GENOMES	ss1360878935	Aug 21, 2014 (142)
41	DDI	ss1428204857	Apr 01, 2015 (144)
42	EVA_GENOME_DK	ss1578387072	Apr 01, 2015 (144)
43	EVA_UK10K_ALSPAC	ss1636792141	Apr 01, 2015 (144)
44	EVA_UK10K_TWINSUK	ss1679786174	Apr 01, 2015 (144)
45	EVA_DECODE	ss1697744871	Apr 01, 2015 (144)
46	EVA_SVP	ss1713622987	Apr 01, 2015 (144)
47	ILLUMINA	ss1752255747	Sep 08, 2015 (146)
48	HAMMER_LAB	ss1809034750	Sep 08, 2015 (146)
49	ILLUMINA	ss1917927023	Feb 12, 2016 (147)
50	WEILL_CORNELL_DGM	ss1937157099	Feb 12, 2016 (147)
51	ILLUMINA	ss1946499482	Feb 12, 2016 (147)
52	ILLUMINA	ss1959801498	Feb 12, 2016 (147)
53	GENOMED	ss1968514725	Jul 19, 2016 (147)
54	JJLAB	ss2029347816	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2157852257	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2221267575	Dec 20, 2016 (150)
57	SYSTEMSBIOZJU	ss2629172098	Nov 08, 2017 (151)
58	GRF	ss2702438200	Nov 08, 2017 (151)
59	GNOMAD	ss2956276848	Nov 08, 2017 (151)
60	AFFY	ss2985116959	Nov 08, 2017 (151)
61	SWEGEN	ss3016467172	Nov 08, 2017 (151)
62	ILLUMINA	ss3021840050	Nov 08, 2017 (151)
63	BIOINF_KMB_FNS_UNIBA	ss3028501484	Nov 08, 2017 (151)
64	CSHL	ss3352005867	Nov 08, 2017 (151)
65	ILLUMINA	ss3627800290	Oct 12, 2018 (152)
66	ILLUMINA	ss3627800291	Oct 12, 2018 (152)
67	ILLUMINA	ss3634704375	Oct 12, 2018 (152)
68	ILLUMINA	ss3638194009	Oct 12, 2018 (152)
69	ILLUMINA	ss3639105014	Oct 12, 2018 (152)
70	ILLUMINA	ss3639560921	Oct 12, 2018 (152)
71	ILLUMINA	ss3640411683	Oct 12, 2018 (152)
72	ILLUMINA	ss3643169969	Oct 12, 2018 (152)
73	ILLUMINA	ss3644705019	Oct 12, 2018 (152)
74	ILLUMINA	ss3652261309	Oct 12, 2018 (152)
75	ILLUMINA	ss3653889142	Oct 12, 2018 (152)
76	EGCUT_WGS	ss3683305730	Jul 13, 2019 (153)
77	EVA_DECODE	ss3701586656	Jul 13, 2019 (153)
78	ILLUMINA	ss3725673751	Jul 13, 2019 (153)
79	ACPOP	ss3742511335	Jul 13, 2019 (153)
80	ILLUMINA	ss3744453753	Jul 13, 2019 (153)
81	ILLUMINA	ss3745004523	Jul 13, 2019 (153)
82	EVA	ss3755342102	Jul 13, 2019 (153)
83	PAGE_CC	ss3771969547	Jul 13, 2019 (153)
84	ILLUMINA	ss3772502034	Jul 13, 2019 (153)
85	KHV_HUMAN_GENOMES	ss3820607185	Jul 13, 2019 (153)
86	EVA	ss3835150707	Apr 27, 2020 (154)
87	EVA	ss3841192524	Apr 27, 2020 (154)
88	EVA	ss3846694519	Apr 27, 2020 (154)
89	HGDP	ss3847582022	Apr 27, 2020 (154)
90	SGDP_PRJ	ss3886944055	Apr 27, 2020 (154)
91	KRGDB	ss3936805881	Apr 27, 2020 (154)
92	KOGIC	ss3980080708	Apr 27, 2020 (154)
93	EVA	ss3984732231	Apr 26, 2021 (155)
94	EVA	ss3985823495	Apr 26, 2021 (155)
95	EVA	ss4017796155	Apr 26, 2021 (155)
96	TOPMED	ss5055408407	Apr 26, 2021 (155)
97	TOMMO_GENOMICS	ss5225007734	Apr 26, 2021 (155)
98	1000G_HIGH_COVERAGE	ss5305167884	Oct 16, 2022 (156)
99	EVA	ss5315930136	Oct 16, 2022 (156)
100	EVA	ss5431187850	Oct 16, 2022 (156)
101	HUGCELL_USP	ss5497951405	Oct 16, 2022 (156)
102	EVA	ss5511924864	Oct 16, 2022 (156)
103	1000G_HIGH_COVERAGE	ss5609944043	Oct 16, 2022 (156)
104	SANFORD_IMAGENETICS	ss5624412878	Oct 16, 2022 (156)
105	SANFORD_IMAGENETICS	ss5661224293	Oct 16, 2022 (156)
106	TOMMO_GENOMICS	ss5782752353	Oct 16, 2022 (156)
107	YY_MCH	ss5817065010	Oct 16, 2022 (156)
108	EVA	ss5827493458	Oct 16, 2022 (156)
109	EVA	ss5847485768	Oct 16, 2022 (156)
110	EVA	ss5847820298	Oct 16, 2022 (156)
111	EVA	ss5852037493	Oct 16, 2022 (156)
112	EVA	ss5873935421	Oct 16, 2022 (156)
113	EVA	ss5952633573	Oct 16, 2022 (156)
114	EVA	ss5979526405	Oct 16, 2022 (156)
115	1000Genomes	NC_000018.9 - 40288293	Oct 12, 2018 (152)
116	1000Genomes_30x	NC_000018.10 - 42708328	Oct 16, 2022 (156)
117	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 40288293	Oct 12, 2018 (152)
118	Genetic variation in the Estonian population	NC_000018.9 - 40288293	Oct 12, 2018 (152)
119	The Danish reference pan genome	NC_000018.9 - 40288293	Apr 27, 2020 (154)
120	gnomAD - Genomes	NC_000018.10 - 42708328	Apr 26, 2021 (155)
121	Genome of the Netherlands Release 5	NC_000018.9 - 40288293	Apr 27, 2020 (154)
122	HGDP-CEPH-db Supplement 1	NC_000018.8 - 38542291	Apr 27, 2020 (154)
123	HapMap	NC_000018.10 - 42708328	Apr 27, 2020 (154)
124	KOREAN population from KRGDB	NC_000018.9 - 40288293	Apr 27, 2020 (154)
125	Korean Genome Project	NC_000018.10 - 42708328	Apr 27, 2020 (154)
126	Northern Sweden	NC_000018.9 - 40288293	Jul 13, 2019 (153)
127	The PAGE Study	NC_000018.10 - 42708328	Jul 13, 2019 (153)
128	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000018.9 - 40288293	Apr 26, 2021 (155)
129	CNV burdens in cranial meningiomas	NC_000018.9 - 40288293	Apr 26, 2021 (155)
130	Qatari	NC_000018.9 - 40288293	Apr 27, 2020 (154)
131	SGDP_PRJ	NC_000018.9 - 40288293	Apr 27, 2020 (154)
132	Siberian	NC_000018.9 - 40288293	Apr 27, 2020 (154)
133	8.3KJPN	NC_000018.9 - 40288293	Apr 26, 2021 (155)
134	14KJPN	NC_000018.10 - 42708328	Oct 16, 2022 (156)
135	TopMed	NC_000018.10 - 42708328	Apr 26, 2021 (155)
136	UK 10K study - Twins	NC_000018.9 - 40288293	Oct 12, 2018 (152)
137	A Vietnamese Genetic Variation Database	NC_000018.9 - 40288293	Jul 13, 2019 (153)
138	ALFA	NC_000018.10 - 42708328	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)
rs59816920	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
43983275, ss3936805881	NC_000018.9:40288292:C:A	NC_000018.10:42708327:C:A	(self)
43983275, ss3936805881	NC_000018.9:40288292:C:G	NC_000018.10:42708327:C:G	(self)
259914, ss110439433, ss114319033, ss117855101, ss169650687, ss171737136, ss203205873, ss208109971, ss282975789, ss287276355, ss292163065, ss825611460, ss1697744871, ss1713622987, ss3639105014, ss3639560921, ss3643169969, ss3847582022	NC_000018.8:38542290:C:T	NC_000018.10:42708327:C:T	(self)
74203328, 41108077, 29043978, 4579783, 18316720, 43983275, 15796200, 1049422, 281783, 19199021, 38961035, 10368611, 82977041, 41108077, 9083295, ss227839046, ss237450430, ss243703104, ss491532919, ss537554010, ss565617912, ss661447816, ss780687029, ss783360572, ss833153589, ss993688328, ss1081471377, ss1360878935, ss1428204857, ss1578387072, ss1636792141, ss1679786174, ss1752255747, ss1809034750, ss1917927023, ss1937157099, ss1946499482, ss1959801498, ss1968514725, ss2029347816, ss2157852257, ss2629172098, ss2702438200, ss2956276848, ss2985116959, ss3016467172, ss3021840050, ss3352005867, ss3627800290, ss3627800291, ss3634704375, ss3638194009, ss3640411683, ss3644705019, ss3652261309, ss3653889142, ss3683305730, ss3742511335, ss3744453753, ss3745004523, ss3755342102, ss3772502034, ss3835150707, ss3841192524, ss3886944055, ss3936805881, ss3984732231, ss3985823495, ss4017796155, ss5225007734, ss5315930136, ss5431187850, ss5511924864, ss5624412878, ss5661224293, ss5827493458, ss5847485768, ss5847820298, ss5952633573, ss5979526405	NC_000018.9:40288292:C:T	NC_000018.10:42708327:C:T	(self)
97469978, 523487130, 1594158, 36458709, 1191016, 116589457, 270954070, 10723838396, ss2221267575, ss3028501484, ss3701586656, ss3725673751, ss3771969547, ss3820607185, ss3846694519, ss3980080708, ss5055408407, ss5305167884, ss5497951405, ss5609944043, ss5782752353, ss5817065010, ss5852037493, ss5873935421	NC_000018.10:42708327:C:T	NC_000018.10:42708327:C:T	(self)
ss12422392	NT_010966.13:21777394:C:T	NC_000018.10:42708327:C:T	(self)
ss66726106, ss67869988, ss68015439, ss70969615, ss71580061, ss75639092, ss79280942, ss84783753, ss103391278, ss122899618, ss154468224, ss155096289, ss159642743, ss172396204, ss174712757	NT_010966.14:21777394:C:T	NC_000018.10:42708327: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 rs8085804

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

rs8085804