Name: rs70
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.

rs70

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:11568079 (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 / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.165684 (43855/264690, TOPMED)
C=0.174764 (24496/140166, GnomAD)
C=0.221663 (27418/123692, ALFA) (+ 18 more)
C=0.17871 (5050/28258, 14KJPN)
C=0.17681 (2963/16758, 8.3KJPN)
C=0.1632 (1045/6404, 1000G_30x)
C=0.1679 (841/5008, 1000G)
C=0.2511 (1125/4480, Estonian)
C=0.2260 (871/3854, ALSPAC)
C=0.2244 (832/3708, TWINSUK)
C=0.2106 (617/2930, KOREAN)
C=0.2140 (392/1832, Korea1K)
C=0.288 (287/998, GoNL)
C=0.252 (196/778, PRJEB37584)
C=0.255 (153/600, NorthernSweden)
C=0.164 (87/530, SGDP_PRJ)
C=0.139 (30/216, Qatari)
C=0.233 (49/210, Vietnamese)
C=0.162 (33/204, HapMap)
C=0.17 (9/54, Siberian)
C=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: THSD7A : Intron Variant
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	128724	C=0.220697	T=0.779303
European	Sub	115046	C=0.229465	T=0.770535
African	Sub	6236	C=0.0936	T=0.9064
African Others	Sub	228	C=0.061	T=0.939
African American	Sub	6008	C=0.0949	T=0.9051
Asian	Sub	232	C=0.284	T=0.716
East Asian	Sub	198	C=0.283	T=0.717
Other Asian	Sub	34	C=0.29	T=0.71
Latin American 1	Sub	484	C=0.147	T=0.853
Latin American 2	Sub	686	C=0.114	T=0.886
South Asian	Sub	150	C=0.247	T=0.753
Other	Sub	5890	C=0.1993	T=0.8007

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=0.165684	T=0.834316
gnomAD - Genomes	Global	Study-wide	140166	C=0.174764	T=0.825236
gnomAD - Genomes	European	Sub	75886	C=0.23057	T=0.76943
gnomAD - Genomes	African	Sub	42014	C=0.09285	T=0.90715
gnomAD - Genomes	American	Sub	13664	C=0.11410	T=0.88590
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.1285	T=0.8715
gnomAD - Genomes	East Asian	Sub	3128	C=0.2369	T=0.7631
gnomAD - Genomes	Other	Sub	2150	C=0.1726	T=0.8274
Allele Frequency Aggregator	Total	Global	123692	C=0.221663	T=0.778337
Allele Frequency Aggregator	European	Sub	111952	C=0.229098	T=0.770902
Allele Frequency Aggregator	African	Sub	5096	C=0.0930	T=0.9070
Allele Frequency Aggregator	Other	Sub	5092	C=0.2050	T=0.7950
Allele Frequency Aggregator	Latin American 2	Sub	686	C=0.114	T=0.886
Allele Frequency Aggregator	Latin American 1	Sub	484	C=0.147	T=0.853
Allele Frequency Aggregator	Asian	Sub	232	C=0.284	T=0.716
Allele Frequency Aggregator	South Asian	Sub	150	C=0.247	T=0.753
14KJPN	JAPANESE	Study-wide	28258	C=0.17871	T=0.82129
8.3KJPN	JAPANESE	Study-wide	16758	C=0.17681	T=0.82319
1000Genomes_30x	Global	Study-wide	6404	C=0.1632	T=0.8368
1000Genomes_30x	African	Sub	1786	C=0.0683	T=0.9317
1000Genomes_30x	Europe	Sub	1266	C=0.2117	T=0.7883
1000Genomes_30x	South Asian	Sub	1202	C=0.2429	T=0.7571
1000Genomes_30x	East Asian	Sub	1170	C=0.2282	T=0.7718
1000Genomes_30x	American	Sub	980	C=0.098	T=0.902
1000Genomes	Global	Study-wide	5008	C=0.1679	T=0.8321
1000Genomes	African	Sub	1322	C=0.0726	T=0.9274
1000Genomes	East Asian	Sub	1008	C=0.2282	T=0.7718
1000Genomes	Europe	Sub	1006	C=0.2048	T=0.7952
1000Genomes	South Asian	Sub	978	C=0.240	T=0.760
1000Genomes	American	Sub	694	C=0.107	T=0.893
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.2511	T=0.7489
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.2260	T=0.7740
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.2244	T=0.7756
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.2106	G=0.0000, T=0.7894
Korean Genome Project	KOREAN	Study-wide	1832	C=0.2140	T=0.7860
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.288	T=0.712
CNV burdens in cranial meningiomas	Global	Study-wide	778	C=0.252	T=0.748
CNV burdens in cranial meningiomas	CRM	Sub	778	C=0.252	T=0.748
Northern Sweden	ACPOP	Study-wide	600	C=0.255	T=0.745
SGDP_PRJ	Global	Study-wide	530	C=0.164	T=0.836
Qatari	Global	Study-wide	216	C=0.139	T=0.861
A Vietnamese Genetic Variation Database	Global	Study-wide	210	C=0.233	T=0.767
HapMap	Global	Study-wide	204	C=0.162	T=0.838
HapMap	American	Sub	116	C=0.207	T=0.793
HapMap	Asian	Sub	88	C=0.10	T=0.90
Siberian	Global	Study-wide	54	C=0.17	T=0.83
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 7	NC_000007.14:g.11568079C>G
GRCh38.p14 chr 7	NC_000007.14:g.11568079C>T
GRCh37.p13 chr 7	NC_000007.13:g.11607706C>G
GRCh37.p13 chr 7	NC_000007.13:g.11607706C>T
THSD7A RefSeqGene	NG_027670.2:g.269119G>C
THSD7A RefSeqGene	NG_027670.2:g.269119G>A
THSD7A RefSeqGene	NG_027670.1:g.269119G>C
THSD7A RefSeqGene	NG_027670.1:g.269119G>A

Gene: THSD7A, thrombospondin type 1 domain containing 7A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
THSD7A transcript	NM_015204.3:c.1453+22381G… NM_015204.3:c.1453+22381G>C	N/A	Intron Variant
THSD7A transcript variant X1	XM_006715659.2:c.1453+223… XM_006715659.2:c.1453+22381G>C	N/A	Intron Variant
THSD7A transcript variant X4	XM_006715660.2:c.1453+223… XM_006715660.2:c.1453+22381G>C	N/A	Intron Variant
THSD7A transcript variant X5	XM_006715662.2:c.1453+223… XM_006715662.2:c.1453+22381G>C	N/A	Intron Variant
THSD7A transcript variant X2	XM_047420039.1:c.1246+223… XM_047420039.1:c.1246+22381G>C	N/A	Intron Variant
THSD7A transcript variant X3	XM_047420040.1:c.1246+223… XM_047420040.1:c.1246+22381G>C	N/A	Intron Variant

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	T
GRCh38.p14 chr 7	NC_000007.14:g.11568079=	NC_000007.14:g.11568079C>G	NC_000007.14:g.11568079C>T
GRCh37.p13 chr 7	NC_000007.13:g.11607706=	NC_000007.13:g.11607706C>G	NC_000007.13:g.11607706C>T
THSD7A RefSeqGene	NG_027670.2:g.269119=	NG_027670.2:g.269119G>C	NG_027670.2:g.269119G>A
THSD7A RefSeqGene	NG_027670.1:g.269119=	NG_027670.1:g.269119G>C	NG_027670.1:g.269119G>A
THSD7A transcript	NM_015204.2:c.1453+22381=	NM_015204.2:c.1453+22381G>C	NM_015204.2:c.1453+22381G>A
THSD7A transcript	NM_015204.3:c.1453+22381=	NM_015204.3:c.1453+22381G>C	NM_015204.3:c.1453+22381G>A
THSD7A transcript variant X1	XM_006715659.2:c.1453+22381=	XM_006715659.2:c.1453+22381G>C	XM_006715659.2:c.1453+22381G>A
THSD7A transcript variant X4	XM_006715660.2:c.1453+22381=	XM_006715660.2:c.1453+22381G>C	XM_006715660.2:c.1453+22381G>A
THSD7A transcript variant X5	XM_006715662.2:c.1453+22381=	XM_006715662.2:c.1453+22381G>C	XM_006715662.2:c.1453+22381G>A
THSD7A transcript variant X2	XM_047420039.1:c.1246+22381=	XM_047420039.1:c.1246+22381G>C	XM_047420039.1:c.1246+22381G>A
THSD7A transcript variant X3	XM_047420040.1:c.1246+22381=	XM_047420040.1:c.1246+22381G>C	XM_047420040.1:c.1246+22381G>A

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#.

109 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss69	Sep 19, 2000 (36)
2	TSC-CSHL	ss3128794	Jun 15, 2001 (96)
3	WI_SSAHASNP	ss11857760	Jul 11, 2003 (116)
4	WUGSC_SSAHASNP	ss14583224	Dec 05, 2003 (120)
5	CSHL-HAPMAP	ss19728302	Feb 27, 2004 (120)
6	SSAHASNP	ss22604685	Apr 05, 2004 (121)
7	SSAHASNP	ss22911781	Apr 05, 2004 (121)
8	HGSV	ss78749484	Dec 06, 2007 (129)
9	BCMHGSC_JDW	ss93628250	Mar 24, 2008 (129)
10	HUMANGENOME_JCVI	ss98132698	Feb 06, 2009 (130)
11	BGI	ss105492539	Feb 06, 2009 (130)
12	1000GENOMES	ss111512756	Jan 25, 2009 (130)
13	1000GENOMES	ss113308428	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss115929956	Feb 14, 2009 (130)
15	ENSEMBL	ss142655633	Dec 01, 2009 (131)
16	ENSEMBL	ss143684984	Dec 01, 2009 (131)
17	GMI	ss158041886	Dec 01, 2009 (131)
18	ILLUMINA	ss160835417	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss162049998	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss163638439	Jul 04, 2010 (132)
21	BUSHMAN	ss202943123	Jul 04, 2010 (132)
22	BCM-HGSC-SUB	ss208242409	Jul 04, 2010 (132)
23	1000GENOMES	ss222903869	Jul 14, 2010 (132)
24	1000GENOMES	ss233847473	Jul 15, 2010 (132)
25	1000GENOMES	ss240827783	Jul 15, 2010 (132)
26	GMI	ss279184103	May 04, 2012 (137)
27	GMI	ss285574015	Apr 25, 2013 (138)
28	PJP	ss293988694	May 09, 2011 (134)
29	ILLUMINA	ss481455323	May 04, 2012 (137)
30	ILLUMINA	ss482435807	Sep 08, 2015 (146)
31	TISHKOFF	ss559802840	Apr 25, 2013 (138)
32	SSMP	ss654151312	Apr 25, 2013 (138)
33	ILLUMINA	ss832460019	Apr 01, 2015 (144)
34	EVA-GONL	ss983943267	Aug 21, 2014 (142)
35	JMKIDD_LAB	ss1074355710	Aug 21, 2014 (142)
36	1000GENOMES	ss1323908228	Aug 21, 2014 (142)
37	DDI	ss1431026859	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1582068408	Apr 01, 2015 (144)
39	EVA_DECODE	ss1593507554	Apr 01, 2015 (144)
40	EVA_UK10K_ALSPAC	ss1617560596	Apr 01, 2015 (144)
41	EVA_UK10K_TWINSUK	ss1660554629	Apr 01, 2015 (144)
42	ILLUMINA	ss1752659958	Sep 08, 2015 (146)
43	HAMMER_LAB	ss1804865038	Sep 08, 2015 (146)
44	WEILL_CORNELL_DGM	ss1927188683	Feb 12, 2016 (147)
45	ILLUMINA	ss1946201783	Feb 12, 2016 (147)
46	ILLUMINA	ss1958987181	Feb 12, 2016 (147)
47	GENOMED	ss1970622856	Jul 19, 2016 (147)
48	JJLAB	ss2024265861	Sep 14, 2016 (149)
49	USC_VALOUEV	ss2152464783	Dec 20, 2016 (150)
50	HUMAN_LONGEVITY	ss2291620152	Dec 20, 2016 (150)
51	SYSTEMSBIOZJU	ss2626622665	Nov 08, 2017 (151)
52	ILLUMINA	ss2634565611	Nov 08, 2017 (151)
53	GRF	ss2708115032	Nov 08, 2017 (151)
54	ILLUMINA	ss2711102864	Nov 08, 2017 (151)
55	GNOMAD	ss2849707735	Nov 08, 2017 (151)
56	SWEGEN	ss3000619874	Nov 08, 2017 (151)
57	ILLUMINA	ss3022707327	Nov 08, 2017 (151)
58	BIOINF_KMB_FNS_UNIBA	ss3025926867	Nov 08, 2017 (151)
59	CSHL	ss3347434289	Nov 08, 2017 (151)
60	ILLUMINA	ss3625921752	Oct 12, 2018 (152)
61	ILLUMINA	ss3633451873	Oct 12, 2018 (152)
62	ILLUMINA	ss3634176293	Oct 12, 2018 (152)
63	ILLUMINA	ss3635107378	Oct 12, 2018 (152)
64	ILLUMINA	ss3635856384	Oct 12, 2018 (152)
65	ILLUMINA	ss3636837325	Oct 12, 2018 (152)
66	ILLUMINA	ss3637609326	Oct 12, 2018 (152)
67	ILLUMINA	ss3640814674	Oct 12, 2018 (152)
68	ILLUMINA	ss3641207949	Oct 12, 2018 (152)
69	ILLUMINA	ss3641505320	Oct 12, 2018 (152)
70	ILLUMINA	ss3644934883	Oct 12, 2018 (152)
71	URBANLAB	ss3648561406	Oct 12, 2018 (152)
72	ILLUMINA	ss3653234815	Oct 12, 2018 (152)
73	EGCUT_WGS	ss3668538578	Jul 13, 2019 (153)
74	EVA_DECODE	ss3719091580	Jul 13, 2019 (153)
75	ILLUMINA	ss3726419504	Jul 13, 2019 (153)
76	ACPOP	ss3734353276	Jul 13, 2019 (153)
77	ILLUMINA	ss3744284947	Jul 13, 2019 (153)
78	ILLUMINA	ss3745407266	Jul 13, 2019 (153)
79	EVA	ss3766181652	Jul 13, 2019 (153)
80	ILLUMINA	ss3772900476	Jul 13, 2019 (153)
81	PACBIO	ss3785733004	Jul 13, 2019 (153)
82	PACBIO	ss3791047262	Jul 13, 2019 (153)
83	PACBIO	ss3795926960	Jul 13, 2019 (153)
84	KHV_HUMAN_GENOMES	ss3809346999	Jul 13, 2019 (153)
85	EVA	ss3830411426	Apr 26, 2020 (154)
86	EVA	ss3838691802	Apr 26, 2020 (154)
87	EVA	ss3844142483	Apr 26, 2020 (154)
88	SGDP_PRJ	ss3866619687	Apr 26, 2020 (154)
89	KRGDB	ss3913646084	Apr 26, 2020 (154)
90	KOGIC	ss3960878240	Apr 26, 2020 (154)
91	EVA	ss3984583194	Apr 26, 2021 (155)
92	EVA	ss4017320067	Apr 26, 2021 (155)
93	TOPMED	ss4735402125	Apr 26, 2021 (155)
94	TOMMO_GENOMICS	ss5181791585	Apr 26, 2021 (155)
95	1000G_HIGH_COVERAGE	ss5271810400	Oct 14, 2022 (156)
96	EVA	ss5315223240	Oct 14, 2022 (156)
97	HUGCELL_USP	ss5469096292	Oct 14, 2022 (156)
98	EVA	ss5508845182	Oct 14, 2022 (156)
99	1000G_HIGH_COVERAGE	ss5559438985	Oct 14, 2022 (156)
100	SANFORD_IMAGENETICS	ss5624654272	Oct 14, 2022 (156)
101	SANFORD_IMAGENETICS	ss5642333741	Oct 14, 2022 (156)
102	TOMMO_GENOMICS	ss5721241023	Oct 14, 2022 (156)
103	YY_MCH	ss5808330019	Oct 14, 2022 (156)
104	EVA	ss5822402107	Oct 14, 2022 (156)
105	EVA	ss5848128070	Oct 14, 2022 (156)
106	EVA	ss5855759938	Oct 14, 2022 (156)
107	EVA	ss5857684438	Oct 14, 2022 (156)
108	EVA	ss5971523735	Oct 14, 2022 (156)
109	EVA	ss5979816355	Oct 14, 2022 (156)
110	1000Genomes	NC_000007.13 - 11607706	Oct 12, 2018 (152)
111	1000Genomes_30x	NC_000007.14 - 11568079	Oct 14, 2022 (156)
112	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 11607706	Oct 12, 2018 (152)
113	Genetic variation in the Estonian population	NC_000007.13 - 11607706	Oct 12, 2018 (152)
114	The Danish reference pan genome	NC_000007.13 - 11607706	Apr 26, 2020 (154)
115	gnomAD - Genomes	NC_000007.14 - 11568079	Apr 26, 2021 (155)
116	Genome of the Netherlands Release 5	NC_000007.13 - 11607706	Apr 26, 2020 (154)
117	HapMap	NC_000007.14 - 11568079	Apr 26, 2020 (154)
118	KOREAN population from KRGDB	NC_000007.13 - 11607706	Apr 26, 2020 (154)
119	Korean Genome Project	NC_000007.14 - 11568079	Apr 26, 2020 (154)
120	Northern Sweden	NC_000007.13 - 11607706	Jul 13, 2019 (153)
121	CNV burdens in cranial meningiomas	NC_000007.13 - 11607706	Apr 26, 2021 (155)
122	Qatari	NC_000007.13 - 11607706	Apr 26, 2020 (154)
123	SGDP_PRJ	NC_000007.13 - 11607706	Apr 26, 2020 (154)
124	Siberian	NC_000007.13 - 11607706	Apr 26, 2020 (154)
125	8.3KJPN	NC_000007.13 - 11607706	Apr 26, 2021 (155)
126	14KJPN	NC_000007.14 - 11568079	Oct 14, 2022 (156)
127	TopMed	NC_000007.14 - 11568079	Apr 26, 2021 (155)
128	UK 10K study - Twins	NC_000007.13 - 11607706	Oct 12, 2018 (152)
129	A Vietnamese Genetic Variation Database	NC_000007.13 - 11607706	Jul 13, 2019 (153)
130	ALFA	NC_000007.14 - 11568079	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)
rs10377676	Feb 27, 2004 (120)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
20823478, ss3913646084	NC_000007.13:11607705:C:G	NC_000007.14:11568078:C:G	(self)
ss78749484	NC_000007.11:11380945:C:T	NC_000007.14:11568078:C:T	(self)
ss93628250, ss111512756, ss113308428, ss115929956, ss162049998, ss163638439, ss202943123, ss208242409, ss279184103, ss285574015, ss293988694, ss1593507554	NC_000007.12:11574230:C:T	NC_000007.14:11568078:C:T	(self)
35835629, 19975693, 14276826, 8233347, 8901448, 20823478, 7638141, 132613, 9230613, 18636667, 4981137, 39760892, 19975693, 4446912, ss222903869, ss233847473, ss240827783, ss481455323, ss482435807, ss559802840, ss654151312, ss832460019, ss983943267, ss1074355710, ss1323908228, ss1431026859, ss1582068408, ss1617560596, ss1660554629, ss1752659958, ss1804865038, ss1927188683, ss1946201783, ss1958987181, ss1970622856, ss2024265861, ss2152464783, ss2626622665, ss2634565611, ss2708115032, ss2711102864, ss2849707735, ss3000619874, ss3022707327, ss3347434289, ss3625921752, ss3633451873, ss3634176293, ss3635107378, ss3635856384, ss3636837325, ss3637609326, ss3640814674, ss3641207949, ss3641505320, ss3644934883, ss3653234815, ss3668538578, ss3734353276, ss3744284947, ss3745407266, ss3766181652, ss3772900476, ss3785733004, ss3791047262, ss3795926960, ss3830411426, ss3838691802, ss3866619687, ss3913646084, ss3984583194, ss4017320067, ss5181791585, ss5315223240, ss5508845182, ss5624654272, ss5642333741, ss5822402107, ss5848128070, ss5971523735, ss5979816355	NC_000007.13:11607705:C:T	NC_000007.14:11568078:C:T	(self)
46964920, 252742071, 3333583, 17256241, 55078127, 572779684, 11607651561, ss2291620152, ss3025926867, ss3648561406, ss3719091580, ss3726419504, ss3809346999, ss3844142483, ss3960878240, ss4735402125, ss5271810400, ss5469096292, ss5559438985, ss5721241023, ss5808330019, ss5855759938, ss5857684438	NC_000007.14:11568078:C:T	NC_000007.14:11568078:C:T	(self)
ss11857760	NT_007819.13:10903378:C:T	NC_000007.14:11568078:C:T	(self)
ss14583224, ss19728302, ss22604685, ss22911781	NT_007819.14:10903378:C:T	NC_000007.14:11568078:C:T	(self)
ss69, ss3128794, ss98132698, ss105492539, ss142655633, ss143684984, ss158041886, ss160835417	NT_007819.17:11597705:C:T	NC_000007.14:11568078: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 rs70

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

rs70