Name: rs8083625
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.

rs8083625

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:24118576 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.282765 (74845/264690, TOPMED)
T=0.285617 (39931/139806, GnomAD)
T=0.31599 (22467/71100, ALFA) (+ 18 more)
T=0.18257 (5159/28258, 14KJPN)
T=0.18300 (3067/16760, 8.3KJPN)
T=0.2687 (1721/6404, 1000G_30x)
T=0.2664 (1334/5008, 1000G)
T=0.3004 (1346/4480, Estonian)
T=0.3191 (1230/3854, ALSPAC)
T=0.3258 (1208/3708, TWINSUK)
T=0.2143 (628/2930, KOREAN)
T=0.3316 (691/2084, HGDP_Stanford)
T=0.2400 (454/1892, HapMap)
T=0.293 (292/998, GoNL)
T=0.337 (202/600, NorthernSweden)
T=0.262 (140/534, MGP)
C=0.408 (107/262, SGDP_PRJ)
T=0.329 (71/216, Qatari)
T=0.19 (10/52, Ancient Sardinia)
T=0.38 (15/40, GENOME_DK)
C=0.39 (11/28, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TTC39C : 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	71100	C=0.68401	T=0.31599
European	Sub	58774	C=0.68268	T=0.31732
African	Sub	4502	C=0.8068	T=0.1932
African Others	Sub	170	C=0.859	T=0.141
African American	Sub	4332	C=0.8047	T=0.1953
Asian	Sub	186	C=0.817	T=0.183
East Asian	Sub	146	C=0.795	T=0.205
Other Asian	Sub	40	C=0.90	T=0.10
Latin American 1	Sub	246	C=0.740	T=0.260
Latin American 2	Sub	1226	C=0.6305	T=0.3695
South Asian	Sub	4954	C=0.5937	T=0.4063
Other	Sub	1212	C=0.6840	T=0.3160

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=0.717235	T=0.282765
gnomAD - Genomes	Global	Study-wide	139806	C=0.714383	T=0.285617
gnomAD - Genomes	European	Sub	75720	C=0.67113	T=0.32887
gnomAD - Genomes	African	Sub	41878	C=0.80484	T=0.19516
gnomAD - Genomes	American	Sub	13616	C=0.66554	T=0.33446
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	C=0.6615	T=0.3385
gnomAD - Genomes	East Asian	Sub	3128	C=0.8235	T=0.1765
gnomAD - Genomes	Other	Sub	2146	C=0.7078	T=0.2922
Allele Frequency Aggregator	Total	Global	71100	C=0.68401	T=0.31599
Allele Frequency Aggregator	European	Sub	58774	C=0.68268	T=0.31732
Allele Frequency Aggregator	South Asian	Sub	4954	C=0.5937	T=0.4063
Allele Frequency Aggregator	African	Sub	4502	C=0.8068	T=0.1932
Allele Frequency Aggregator	Latin American 2	Sub	1226	C=0.6305	T=0.3695
Allele Frequency Aggregator	Other	Sub	1212	C=0.6840	T=0.3160
Allele Frequency Aggregator	Latin American 1	Sub	246	C=0.740	T=0.260
Allele Frequency Aggregator	Asian	Sub	186	C=0.817	T=0.183
14KJPN	JAPANESE	Study-wide	28258	C=0.81743	T=0.18257
8.3KJPN	JAPANESE	Study-wide	16760	C=0.81700	T=0.18300
1000Genomes_30x	Global	Study-wide	6404	C=0.7313	T=0.2687
1000Genomes_30x	African	Sub	1786	C=0.8471	T=0.1529
1000Genomes_30x	Europe	Sub	1266	C=0.6635	T=0.3365
1000Genomes_30x	South Asian	Sub	1202	C=0.6098	T=0.3902
1000Genomes_30x	East Asian	Sub	1170	C=0.8342	T=0.1658
1000Genomes_30x	American	Sub	980	C=0.634	T=0.366
1000Genomes	Global	Study-wide	5008	C=0.7336	T=0.2664
1000Genomes	African	Sub	1322	C=0.8457	T=0.1543
1000Genomes	East Asian	Sub	1008	C=0.8413	T=0.1587
1000Genomes	Europe	Sub	1006	C=0.6680	T=0.3320
1000Genomes	South Asian	Sub	978	C=0.607	T=0.393
1000Genomes	American	Sub	694	C=0.637	T=0.363
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.6996	T=0.3004
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6809	T=0.3191
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6742	T=0.3258
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.7857	T=0.2143
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.6684	T=0.3316
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.791	T=0.209
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.568	T=0.432
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.631	T=0.369
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.653	T=0.347
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.781	T=0.219
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.468	T=0.532
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.92	T=0.08
HapMap	Global	Study-wide	1892	C=0.7600	T=0.2400
HapMap	American	Sub	770	C=0.656	T=0.344
HapMap	African	Sub	692	C=0.863	T=0.137
HapMap	Asian	Sub	254	C=0.815	T=0.185
HapMap	Europe	Sub	176	C=0.733	T=0.267
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.707	T=0.293
Northern Sweden	ACPOP	Study-wide	600	C=0.663	T=0.337
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	C=0.738	T=0.262
SGDP_PRJ	Global	Study-wide	262	C=0.408	T=0.592
Qatari	Global	Study-wide	216	C=0.671	T=0.329
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	52	C=0.81	T=0.19
The Danish reference pan genome	Danish	Study-wide	40	C=0.62	T=0.38
Siberian	Global	Study-wide	28	C=0.39	T=0.61

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.24118576C>T
GRCh37.p13 chr 18	NC_000018.9:g.21698540C>T

Gene: TTC39C, tetratricopeptide repeat domain 39C (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TTC39C transcript variant 1	NM_001135993.2:c.1186+344… NM_001135993.2:c.1186+344C>T	N/A	Intron Variant
TTC39C transcript variant 4	NM_001292030.2:c.265+344C… NM_001292030.2:c.265+344C>T	N/A	Intron Variant
TTC39C transcript variant 2	NM_153211.4:c.1003+344C>T	N/A	Intron Variant
TTC39C transcript variant 3	NM_001243425.2:c.	N/A	Genic Downstream Transcript Variant
TTC39C transcript variant X2	XM_011525814.4:c.1078+392… XM_011525814.4:c.1078+3929C>T	N/A	Intron Variant
TTC39C transcript variant X1	XM_047437296.1:c.1087+344… XM_047437296.1:c.1087+344C>T	N/A	Intron Variant
TTC39C transcript variant X3	XM_047437297.1:c.1003+344… XM_047437297.1:c.1003+344C>T	N/A	Intron Variant
TTC39C transcript variant X4	XM_047437298.1:c.1003+344… XM_047437298.1:c.1003+344C>T	N/A	Intron Variant
TTC39C transcript variant X5	XM_006722392.4:c.	N/A	Genic Downstream Transcript 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=	T
GRCh38.p14 chr 18	NC_000018.10:g.24118576=	NC_000018.10:g.24118576C>T
GRCh37.p13 chr 18	NC_000018.9:g.21698540=	NC_000018.9:g.21698540C>T
TTC39C transcript variant 1	NM_001135993.1:c.1186+344=	NM_001135993.1:c.1186+344C>T
TTC39C transcript variant 1	NM_001135993.2:c.1186+344=	NM_001135993.2:c.1186+344C>T
TTC39C transcript variant 4	NM_001292030.2:c.265+344=	NM_001292030.2:c.265+344C>T
TTC39C transcript variant 2	NM_153211.3:c.1003+344=	NM_153211.3:c.1003+344C>T
TTC39C transcript variant 2	NM_153211.4:c.1003+344=	NM_153211.4:c.1003+344C>T
TTC39C transcript variant X1	XM_005258198.1:c.1003+344=	XM_005258198.1:c.1003+344C>T
TTC39C transcript variant X2	XM_011525814.4:c.1078+3929=	XM_011525814.4:c.1078+3929C>T
TTC39C transcript variant X1	XM_047437296.1:c.1087+344=	XM_047437296.1:c.1087+344C>T
TTC39C transcript variant X3	XM_047437297.1:c.1003+344=	XM_047437297.1:c.1003+344C>T
TTC39C transcript variant X4	XM_047437298.1:c.1003+344=	XM_047437298.1:c.1003+344C>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#.

98 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	WI_SSAHASNP	ss12418186	Jul 11, 2003 (116)
2	ABI	ss44133948	Mar 15, 2006 (126)
3	ILLUMINA	ss66726090	Dec 02, 2006 (127)
4	ILLUMINA	ss67869714	Dec 02, 2006 (127)
5	ILLUMINA	ss68015258	Dec 02, 2006 (127)
6	ILLUMINA	ss70969478	May 25, 2008 (130)
7	ILLUMINA	ss71579880	May 18, 2007 (127)
8	ILLUMINA	ss75644684	Dec 06, 2007 (129)
9	HGSV	ss77292242	Dec 06, 2007 (129)
10	ILLUMINA	ss79280860	Dec 15, 2007 (130)
11	KRIBB_YJKIM	ss84783360	Dec 15, 2007 (130)
12	HUMANGENOME_JCVI	ss96497773	Feb 05, 2009 (130)
13	1000GENOMES	ss110232819	Jan 24, 2009 (130)
14	ILLUMINA	ss122899129	Dec 01, 2009 (131)
15	ENSEMBL	ss144198133	Dec 01, 2009 (131)
16	ILLUMINA	ss154468083	Dec 01, 2009 (131)
17	GMI	ss154933743	Dec 01, 2009 (131)
18	ILLUMINA	ss159642603	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss171586675	Jul 04, 2010 (132)
20	ILLUMINA	ss172395856	Jul 04, 2010 (132)
21	ILLUMINA	ss174711635	Jul 04, 2010 (132)
22	BUSHMAN	ss203049618	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss208124525	Jul 04, 2010 (132)
24	1000GENOMES	ss227768843	Jul 14, 2010 (132)
25	1000GENOMES	ss237401430	Jul 15, 2010 (132)
26	1000GENOMES	ss243665430	Jul 15, 2010 (132)
27	GMI	ss282929982	May 04, 2012 (137)
28	GMI	ss287255465	Apr 25, 2013 (138)
29	PJP	ss292139923	May 09, 2011 (134)
30	CLINSEQ_SNP	ss491748714	May 04, 2012 (137)
31	SSMP	ss661368529	Apr 25, 2013 (138)
32	ILLUMINA	ss825611378	Apr 01, 2015 (144)
33	ILLUMINA	ss833153449	Jul 13, 2019 (153)
34	EVA-GONL	ss993552162	Aug 21, 2014 (142)
35	JMKIDD_LAB	ss1081370297	Aug 21, 2014 (142)
36	1000GENOMES	ss1360364742	Aug 21, 2014 (142)
37	DDI	ss1428166564	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1578334113	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1636517679	Apr 01, 2015 (144)
40	EVA_UK10K_TWINSUK	ss1679511712	Apr 01, 2015 (144)
41	EVA_DECODE	ss1697605462	Apr 01, 2015 (144)
42	EVA_MGP	ss1711483143	Apr 01, 2015 (144)
43	EVA_SVP	ss1713613275	Apr 01, 2015 (144)
44	HAMMER_LAB	ss1808980808	Sep 08, 2015 (146)
45	WEILL_CORNELL_DGM	ss1937029044	Feb 12, 2016 (147)
46	GENOMED	ss1968483652	Jul 19, 2016 (147)
47	JJLAB	ss2029283122	Sep 14, 2016 (149)
48	USC_VALOUEV	ss2157784296	Dec 20, 2016 (150)
49	HUMAN_LONGEVITY	ss2220180629	Dec 20, 2016 (150)
50	GRF	ss2702367131	Nov 08, 2017 (151)
51	GNOMAD	ss2954810872	Nov 08, 2017 (151)
52	SWEGEN	ss3016268627	Nov 08, 2017 (151)
53	BIOINF_KMB_FNS_UNIBA	ss3028467482	Nov 08, 2017 (151)
54	CSHL	ss3351949662	Nov 08, 2017 (151)
55	ILLUMINA	ss3638186774	Oct 12, 2018 (152)
56	ILLUMINA	ss3639101286	Oct 12, 2018 (152)
57	ILLUMINA	ss3639558555	Oct 12, 2018 (152)
58	ILLUMINA	ss3641087922	Oct 12, 2018 (152)
59	ILLUMINA	ss3641383451	Oct 12, 2018 (152)
60	ILLUMINA	ss3643163176	Oct 12, 2018 (152)
61	URBANLAB	ss3650757578	Oct 12, 2018 (152)
62	EGCUT_WGS	ss3683092687	Jul 13, 2019 (153)
63	EVA_DECODE	ss3701341766	Jul 13, 2019 (153)
64	ACPOP	ss3742402793	Jul 13, 2019 (153)
65	EVA	ss3755187722	Jul 13, 2019 (153)
66	PACBIO	ss3788329396	Jul 13, 2019 (153)
67	PACBIO	ss3793267099	Jul 13, 2019 (153)
68	PACBIO	ss3798153390	Jul 13, 2019 (153)
69	KHV_HUMAN_GENOMES	ss3820456298	Jul 13, 2019 (153)
70	EVA	ss3825914064	Apr 27, 2020 (154)
71	EVA	ss3835089201	Apr 27, 2020 (154)
72	EVA	ss3841159940	Apr 27, 2020 (154)
73	EVA	ss3846661209	Apr 27, 2020 (154)
74	HGDP	ss3847577436	Apr 27, 2020 (154)
75	SGDP_PRJ	ss3886681173	Apr 27, 2020 (154)
76	KRGDB	ss3936521165	Apr 27, 2020 (154)
77	FSA-LAB	ss3984130989	Apr 27, 2021 (155)
78	EVA	ss3985815598	Apr 27, 2021 (155)
79	EVA	ss3986755040	Apr 27, 2021 (155)
80	EVA	ss4017789268	Apr 27, 2021 (155)
81	TOPMED	ss5050760698	Apr 27, 2021 (155)
82	TOMMO_GENOMICS	ss5224443181	Apr 27, 2021 (155)
83	EVA	ss5237242649	Apr 27, 2021 (155)
84	1000G_HIGH_COVERAGE	ss5304723956	Oct 16, 2022 (156)
85	HUGCELL_USP	ss5497548547	Oct 16, 2022 (156)
86	EVA	ss5511876518	Oct 16, 2022 (156)
87	1000G_HIGH_COVERAGE	ss5609246100	Oct 16, 2022 (156)
88	EVA	ss5624079577	Oct 16, 2022 (156)
89	SANFORD_IMAGENETICS	ss5660971962	Oct 16, 2022 (156)
90	TOMMO_GENOMICS	ss5782026029	Oct 16, 2022 (156)
91	EVA	ss5799460657	Oct 16, 2022 (156)
92	YY_MCH	ss5816959000	Oct 16, 2022 (156)
93	EVA	ss5827322097	Oct 16, 2022 (156)
94	EVA	ss5848466501	Oct 16, 2022 (156)
95	EVA	ss5851985859	Oct 16, 2022 (156)
96	EVA	ss5873415324	Oct 16, 2022 (156)
97	EVA	ss5936570216	Oct 16, 2022 (156)
98	EVA	ss5952365066	Oct 16, 2022 (156)
99	1000Genomes	NC_000018.9 - 21698540	Oct 12, 2018 (152)
100	1000Genomes_30x	NC_000018.10 - 24118576	Oct 16, 2022 (156)
101	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 21698540	Oct 12, 2018 (152)
102	Genetic variation in the Estonian population	NC_000018.9 - 21698540	Oct 12, 2018 (152)
103	The Danish reference pan genome	NC_000018.9 - 21698540	Apr 27, 2020 (154)
104	gnomAD - Genomes	NC_000018.10 - 24118576	Apr 27, 2021 (155)
105	Genome of the Netherlands Release 5	NC_000018.9 - 21698540	Apr 27, 2020 (154)
106	HGDP-CEPH-db Supplement 1	NC_000018.8 - 19952538	Apr 27, 2020 (154)
107	HapMap	NC_000018.10 - 24118576	Apr 27, 2020 (154)
108	KOREAN population from KRGDB	NC_000018.9 - 21698540	Apr 27, 2020 (154)
109	Medical Genome Project healthy controls from Spanish population	NC_000018.9 - 21698540	Apr 27, 2020 (154)
110	Northern Sweden	NC_000018.9 - 21698540	Jul 13, 2019 (153)
111	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000018.9 - 21698540	Apr 27, 2021 (155)
112	Qatari	NC_000018.9 - 21698540	Apr 27, 2020 (154)
113	SGDP_PRJ	NC_000018.9 - 21698540	Apr 27, 2020 (154)
114	Siberian	NC_000018.9 - 21698540	Apr 27, 2020 (154)
115	8.3KJPN	NC_000018.9 - 21698540	Apr 27, 2021 (155)
116	14KJPN	NC_000018.10 - 24118576	Oct 16, 2022 (156)
117	TopMed	NC_000018.10 - 24118576	Apr 27, 2021 (155)
118	UK 10K study - Twins	NC_000018.9 - 21698540	Oct 12, 2018 (152)
119	ALFA	NC_000018.10 - 24118576	Apr 27, 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)
rs59564286	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
255328, ss77292242, ss110232819, ss171586675, ss203049618, ss208124525, ss282929982, ss287255465, ss292139923, ss491748714, ss825611378, ss1697605462, ss1713613275, ss3639101286, ss3639558555, ss3643163176, ss3847577436	NC_000018.8:19952537:C:T	NC_000018.10:24118575:C:T	(self)
73670872, 40806796, 28830935, 4529012, 18183093, 43698559, 598903, 15687658, 1041525, 19070966, 38698153, 10300650, 82412488, 40806796, ss227768843, ss237401430, ss243665430, ss661368529, ss833153449, ss993552162, ss1081370297, ss1360364742, ss1428166564, ss1578334113, ss1636517679, ss1679511712, ss1711483143, ss1808980808, ss1937029044, ss1968483652, ss2029283122, ss2157784296, ss2702367131, ss2954810872, ss3016268627, ss3351949662, ss3638186774, ss3641087922, ss3641383451, ss3683092687, ss3742402793, ss3755187722, ss3788329396, ss3793267099, ss3798153390, ss3825914064, ss3835089201, ss3841159940, ss3886681173, ss3936521165, ss3984130989, ss3985815598, ss3986755040, ss4017789268, ss5224443181, ss5511876518, ss5624079577, ss5660971962, ss5799460657, ss5827322097, ss5848466501, ss5936570216, ss5952365066	NC_000018.9:21698539:C:T	NC_000018.10:24118575:C:T	(self)
96772035, 519719647, 1564141, 115863133, 266306361, 15535666708, ss2220180629, ss3028467482, ss3650757578, ss3701341766, ss3820456298, ss3846661209, ss5050760698, ss5237242649, ss5304723956, ss5497548547, ss5609246100, ss5782026029, ss5816959000, ss5851985859, ss5873415324	NC_000018.10:24118575:C:T	NC_000018.10:24118575:C:T	(self)
ss12418186	NT_010966.13:3187641:C:T	NC_000018.10:24118575:C:T	(self)
ss44133948, ss66726090, ss67869714, ss68015258, ss70969478, ss71579880, ss75644684, ss79280860, ss84783360, ss96497773, ss122899129, ss144198133, ss154468083, ss154933743, ss159642603, ss172395856, ss174711635	NT_010966.14:3187641:C:T	NC_000018.10:24118575: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 rs8083625

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

rs8083625