Name: rs3744856
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.

rs3744856

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:69841693 (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>A / T>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.338951 (89717/264690, TOPMED)
C=0.354258 (56237/158746, ALFA)
C=0.353529 (49511/140048, GnomAD) (+ 19 more)
C=0.23381 (6607/28258, 14KJPN)
C=0.23544 (3946/16760, 8.3KJPN)
C=0.3253 (2083/6404, 1000G_30x)
C=0.3187 (1596/5008, 1000G)
C=0.3551 (1591/4480, Estonian)
C=0.3578 (1379/3854, ALSPAC)
C=0.3579 (1327/3708, TWINSUK)
C=0.2867 (840/2930, KOREAN)
C=0.3085 (583/1890, HapMap)
C=0.2817 (516/1832, Korea1K)
C=0.394 (393/998, GoNL)
C=0.375 (225/600, NorthernSweden)
C=0.322 (172/534, MGP)
T=0.402 (103/256, SGDP_PRJ)
C=0.361 (78/216, Qatari)
C=0.176 (38/216, Vietnamese)
C=0.41 (22/54, Ancient Sardinia)
C=0.38 (15/40, GENOME_DK)
T=0.37 (11/30, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DOK6 : 3 Prime UTR 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	158746	T=0.645742	A=0.000000, C=0.354258
European	Sub	139508	T=0.642178	A=0.000000, C=0.357822
African	Sub	9000	T=0.6500	A=0.0000, C=0.3500
African Others	Sub	320	T=0.678	A=0.000, C=0.322
African American	Sub	8680	T=0.6490	A=0.0000, C=0.3510
Asian	Sub	672	T=0.790	A=0.000, C=0.210
East Asian	Sub	542	T=0.779	A=0.000, C=0.221
Other Asian	Sub	130	T=0.838	A=0.000, C=0.162
Latin American 1	Sub	692	T=0.650	A=0.000, C=0.350
Latin American 2	Sub	2264	T=0.7686	A=0.0000, C=0.2314
South Asian	Sub	184	T=0.679	A=0.000, C=0.321
Other	Sub	6426	T=0.6573	A=0.0000, C=0.3427

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	T=0.661049	C=0.338951
Allele Frequency Aggregator	Total	Global	158746	T=0.645742	A=0.000000, C=0.354258
Allele Frequency Aggregator	European	Sub	139508	T=0.642178	A=0.000000, C=0.357822
Allele Frequency Aggregator	African	Sub	9000	T=0.6500	A=0.0000, C=0.3500
Allele Frequency Aggregator	Other	Sub	6426	T=0.6573	A=0.0000, C=0.3427
Allele Frequency Aggregator	Latin American 2	Sub	2264	T=0.7686	A=0.0000, C=0.2314
Allele Frequency Aggregator	Latin American 1	Sub	692	T=0.650	A=0.000, C=0.350
Allele Frequency Aggregator	Asian	Sub	672	T=0.790	A=0.000, C=0.210
Allele Frequency Aggregator	South Asian	Sub	184	T=0.679	A=0.000, C=0.321
gnomAD - Genomes	Global	Study-wide	140048	T=0.646471	C=0.353529
gnomAD - Genomes	European	Sub	75852	T=0.62854	C=0.37146
gnomAD - Genomes	African	Sub	41958	T=0.63606	C=0.36394
gnomAD - Genomes	American	Sub	13648	T=0.71681	C=0.28319
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	T=0.7566	C=0.2434
gnomAD - Genomes	East Asian	Sub	3116	T=0.7818	C=0.2182
gnomAD - Genomes	Other	Sub	2150	T=0.6693	C=0.3307
14KJPN	JAPANESE	Study-wide	28258	T=0.76619	C=0.23381
8.3KJPN	JAPANESE	Study-wide	16760	T=0.76456	C=0.23544
1000Genomes_30x	Global	Study-wide	6404	T=0.6747	C=0.3253
1000Genomes_30x	African	Sub	1786	T=0.6142	C=0.3858
1000Genomes_30x	Europe	Sub	1266	T=0.6430	C=0.3570
1000Genomes_30x	South Asian	Sub	1202	T=0.6764	C=0.3236
1000Genomes_30x	East Asian	Sub	1170	T=0.7658	C=0.2342
1000Genomes_30x	American	Sub	980	T=0.715	C=0.285
1000Genomes	Global	Study-wide	5008	T=0.6813	C=0.3187
1000Genomes	African	Sub	1322	T=0.6180	C=0.3820
1000Genomes	East Asian	Sub	1008	T=0.7679	C=0.2321
1000Genomes	Europe	Sub	1006	T=0.6392	C=0.3608
1000Genomes	South Asian	Sub	978	T=0.685	C=0.315
1000Genomes	American	Sub	694	T=0.732	C=0.268
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6449	C=0.3551
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6422	C=0.3578
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6421	C=0.3579
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.7133	C=0.2867
HapMap	Global	Study-wide	1890	T=0.6915	C=0.3085
HapMap	American	Sub	768	T=0.701	C=0.299
HapMap	African	Sub	692	T=0.663	C=0.337
HapMap	Asian	Sub	254	T=0.787	C=0.213
HapMap	Europe	Sub	176	T=0.625	C=0.375
Korean Genome Project	KOREAN	Study-wide	1832	T=0.7183	C=0.2817
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.606	C=0.394
Northern Sweden	ACPOP	Study-wide	600	T=0.625	C=0.375
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.678	C=0.322
SGDP_PRJ	Global	Study-wide	256	T=0.402	C=0.598
Qatari	Global	Study-wide	216	T=0.639	C=0.361
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.824	C=0.176
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	54	T=0.59	C=0.41
The Danish reference pan genome	Danish	Study-wide	40	T=0.62	C=0.38
Siberian	Global	Study-wide	30	T=0.37	C=0.63

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.69841693T>A
GRCh38.p14 chr 18	NC_000018.10:g.69841693T>C
GRCh37.p13 chr 18	NC_000018.9:g.67508929T>A
GRCh37.p13 chr 18	NC_000018.9:g.67508929T>C

Gene: DOK6, docking protein 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DOK6 transcript	NM_152721.6:c.*310=	N/A	3 Prime UTR Variant
DOK6 transcript variant X1	XM_017025610.2:c.*310=	N/A	3 Prime UTR Variant
DOK6 transcript variant X2	XM_017025611.2:c.*310=	N/A	3 Prime UTR 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	T=	A	C
GRCh38.p14 chr 18	NC_000018.10:g.69841693=	NC_000018.10:g.69841693T>A	NC_000018.10:g.69841693T>C
GRCh37.p13 chr 18	NC_000018.9:g.67508929=	NC_000018.9:g.67508929T>A	NC_000018.9:g.67508929T>C
DOK6 transcript	NM_152721.6:c.*310=	NM_152721.6:c.*310T>A	NM_152721.6:c.*310T>C
DOK6 transcript	NM_152721.5:c.*310=	NM_152721.5:c.*310T>A	NM_152721.5:c.*310T>C
DOK6 transcript variant X1	XM_017025610.2:c.*310=	XM_017025610.2:c.*310T>A	XM_017025610.2:c.*310T>C
DOK6 transcript variant X2	XM_017025611.2:c.*310=	XM_017025611.2:c.*310T>A	XM_017025611.2:c.*310T>C

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#.

117 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4930864	Aug 28, 2002 (107)
2	WI_SSAHASNP	ss14418517	Dec 05, 2003 (119)
3	SSAHASNP	ss21504358	Apr 05, 2004 (121)
4	PERLEGEN	ss24509671	Sep 20, 2004 (123)
5	ABI	ss44138052	Mar 14, 2006 (126)
6	ILLUMINA	ss65734324	Oct 14, 2006 (127)
7	ILLUMINA	ss75005284	Dec 07, 2007 (129)
8	HGSV	ss80890731	Dec 15, 2007 (130)
9	HGSV	ss86012590	Dec 15, 2007 (130)
10	BCMHGSC_JDW	ss90843085	Mar 24, 2008 (129)
11	HUMANGENOME_JCVI	ss96522095	Feb 05, 2009 (130)
12	1000GENOMES	ss110795333	Jan 25, 2009 (130)
13	1000GENOMES	ss114596610	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss117930045	Feb 14, 2009 (130)
15	KRIBB_YJKIM	ss119458943	Dec 01, 2009 (131)
16	WTCCC	ss120253495	Dec 01, 2009 (131)
17	ENSEMBL	ss136364754	Dec 01, 2009 (131)
18	ENSEMBL	ss137458532	Dec 01, 2009 (131)
19	ILLUMINA	ss160635085	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss168462875	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss170203666	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss171955118	Jul 04, 2010 (132)
23	ILLUMINA	ss173620167	Jul 04, 2010 (132)
24	BUSHMAN	ss203453339	Jul 04, 2010 (132)
25	BCM-HGSC-SUB	ss208224428	Jul 04, 2010 (132)
26	1000GENOMES	ss227950400	Jul 14, 2010 (132)
27	1000GENOMES	ss237533119	Jul 15, 2010 (132)
28	1000GENOMES	ss243768987	Jul 15, 2010 (132)
29	BL	ss255771625	May 09, 2011 (134)
30	GMI	ss283054003	May 04, 2012 (137)
31	PJP	ss292101117	May 09, 2011 (134)
32	ILLUMINA	ss480811179	May 04, 2012 (137)
33	ILLUMINA	ss480826800	May 04, 2012 (137)
34	ILLUMINA	ss481755174	Sep 08, 2015 (146)
35	ILLUMINA	ss485200383	May 04, 2012 (137)
36	ILLUMINA	ss537187158	Sep 08, 2015 (146)
37	TISHKOFF	ss565743442	Apr 25, 2013 (138)
38	SSMP	ss661583960	Apr 25, 2013 (138)
39	ILLUMINA	ss778894143	Aug 21, 2014 (142)
40	ILLUMINA	ss783046192	Aug 21, 2014 (142)
41	ILLUMINA	ss784005065	Aug 21, 2014 (142)
42	ILLUMINA	ss832303977	Apr 01, 2015 (144)
43	ILLUMINA	ss834355304	Aug 21, 2014 (142)
44	EVA-GONL	ss993901980	Aug 21, 2014 (142)
45	JMKIDD_LAB	ss1081631430	Aug 21, 2014 (142)
46	1000GENOMES	ss1361667676	Aug 21, 2014 (142)
47	DDI	ss1428273896	Apr 01, 2015 (144)
48	EVA_GENOME_DK	ss1578476793	Apr 01, 2015 (144)
49	EVA_UK10K_ALSPAC	ss1637224443	Apr 01, 2015 (144)
50	EVA_UK10K_TWINSUK	ss1680218476	Apr 01, 2015 (144)
51	EVA_DECODE	ss1697965410	Apr 01, 2015 (144)
52	EVA_MGP	ss1711489004	Apr 01, 2015 (144)
53	EVA_SVP	ss1713638916	Apr 01, 2015 (144)
54	ILLUMINA	ss1752265786	Sep 08, 2015 (146)
55	HAMMER_LAB	ss1809125691	Sep 08, 2015 (146)
56	WEILL_CORNELL_DGM	ss1937370219	Feb 12, 2016 (147)
57	JJLAB	ss2029459226	Sep 14, 2016 (149)
58	ILLUMINA	ss2094897678	Dec 20, 2016 (150)
59	ILLUMINA	ss2095081701	Dec 20, 2016 (150)
60	USC_VALOUEV	ss2157966584	Dec 20, 2016 (150)
61	HUMAN_LONGEVITY	ss2222902543	Dec 20, 2016 (150)
62	SYSTEMSBIOZJU	ss2629228396	Nov 08, 2017 (151)
63	ILLUMINA	ss2633493896	Nov 08, 2017 (151)
64	GRF	ss2702562371	Nov 08, 2017 (151)
65	ILLUMINA	ss2710872096	Nov 08, 2017 (151)
66	GNOMAD	ss2958485380	Nov 08, 2017 (151)
67	SWEGEN	ss3016789127	Nov 08, 2017 (151)
68	BIOINF_KMB_FNS_UNIBA	ss3028559969	Nov 08, 2017 (151)
69	CSHL	ss3352102277	Nov 08, 2017 (151)
70	ILLUMINA	ss3627846322	Oct 12, 2018 (152)
71	ILLUMINA	ss3631469533	Oct 12, 2018 (152)
72	ILLUMINA	ss3633168600	Oct 12, 2018 (152)
73	ILLUMINA	ss3633877616	Oct 12, 2018 (152)
74	ILLUMINA	ss3634713236	Oct 12, 2018 (152)
75	ILLUMINA	ss3635564772	Oct 12, 2018 (152)
76	ILLUMINA	ss3636403762	Oct 12, 2018 (152)
77	ILLUMINA	ss3637316424	Oct 12, 2018 (152)
78	ILLUMINA	ss3638205276	Oct 12, 2018 (152)
79	ILLUMINA	ss3640420544	Oct 12, 2018 (152)
80	ILLUMINA	ss3643180330	Oct 12, 2018 (152)
81	OMUKHERJEE_ADBS	ss3646524627	Oct 12, 2018 (152)
82	URBANLAB	ss3650827091	Oct 12, 2018 (152)
83	ILLUMINA	ss3652279656	Oct 12, 2018 (152)
84	EGCUT_WGS	ss3683641616	Jul 13, 2019 (153)
85	EVA_DECODE	ss3701979976	Jul 13, 2019 (153)
86	ACPOP	ss3742691055	Jul 13, 2019 (153)
87	ILLUMINA	ss3745013345	Jul 13, 2019 (153)
88	EVA	ss3755592307	Jul 13, 2019 (153)
89	ILLUMINA	ss3772510799	Jul 13, 2019 (153)
90	KHV_HUMAN_GENOMES	ss3820849228	Jul 13, 2019 (153)
91	EVA	ss3825917672	Apr 27, 2020 (154)
92	EVA	ss3835255123	Apr 27, 2020 (154)
93	EVA	ss3841247637	Apr 27, 2020 (154)
94	EVA	ss3846750642	Apr 27, 2020 (154)
95	SGDP_PRJ	ss3887357664	Apr 27, 2020 (154)
96	KRGDB	ss3937257325	Apr 27, 2020 (154)
97	KOGIC	ss3980453698	Apr 27, 2020 (154)
98	FSA-LAB	ss3984134783	Apr 26, 2021 (155)
99	EVA	ss3985836674	Apr 26, 2021 (155)
100	EVA	ss3986078090	Apr 26, 2021 (155)
101	EVA	ss4017806763	Apr 26, 2021 (155)
102	TOPMED	ss5062326706	Apr 26, 2021 (155)
103	TOMMO_GENOMICS	ss5225887785	Apr 26, 2021 (155)
104	1000G_HIGH_COVERAGE	ss5305855091	Oct 16, 2022 (156)
105	EVA	ss5315946146	Oct 16, 2022 (156)
106	EVA	ss5432452160	Oct 16, 2022 (156)
107	HUGCELL_USP	ss5498572598	Oct 16, 2022 (156)
108	1000G_HIGH_COVERAGE	ss5610988071	Oct 16, 2022 (156)
109	SANFORD_IMAGENETICS	ss5661620228	Oct 16, 2022 (156)
110	TOMMO_GENOMICS	ss5783883079	Oct 16, 2022 (156)
111	EVA	ss5799998592	Oct 16, 2022 (156)
112	YY_MCH	ss5817241888	Oct 16, 2022 (156)
113	EVA	ss5827770317	Oct 16, 2022 (156)
114	EVA	ss5852127383	Oct 16, 2022 (156)
115	EVA	ss5874734891	Oct 16, 2022 (156)
116	EVA	ss5953051031	Oct 16, 2022 (156)
117	EVA	ss5981015508	Oct 16, 2022 (156)
118	1000Genomes	NC_000018.9 - 67508929	Oct 12, 2018 (152)
119	1000Genomes_30x	NC_000018.10 - 69841693	Oct 16, 2022 (156)
120	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 67508929	Oct 12, 2018 (152)
121	Genetic variation in the Estonian population	NC_000018.9 - 67508929	Oct 12, 2018 (152)
122	The Danish reference pan genome	NC_000018.9 - 67508929	Apr 27, 2020 (154)
123	gnomAD - Genomes	NC_000018.10 - 69841693	Apr 26, 2021 (155)
124	Genome of the Netherlands Release 5	NC_000018.9 - 67508929	Apr 27, 2020 (154)
125	HapMap	NC_000018.10 - 69841693	Apr 27, 2020 (154)
126	KOREAN population from KRGDB	NC_000018.9 - 67508929	Apr 27, 2020 (154)
127	Korean Genome Project	NC_000018.10 - 69841693	Apr 27, 2020 (154)
128	Medical Genome Project healthy controls from Spanish population	NC_000018.9 - 67508929	Apr 27, 2020 (154)
129	Northern Sweden	NC_000018.9 - 67508929	Jul 13, 2019 (153)
130	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000018.9 - 67508929	Apr 26, 2021 (155)
131	Qatari	NC_000018.9 - 67508929	Apr 27, 2020 (154)
132	SGDP_PRJ	NC_000018.9 - 67508929	Apr 27, 2020 (154)
133	Siberian	NC_000018.9 - 67508929	Apr 27, 2020 (154)
134	8.3KJPN	NC_000018.9 - 67508929	Apr 26, 2021 (155)
135	14KJPN	NC_000018.10 - 69841693	Oct 16, 2022 (156)
136	TopMed	NC_000018.10 - 69841693	Apr 26, 2021 (155)
137	UK 10K study - Twins	NC_000018.9 - 67508929	Oct 12, 2018 (152)
138	A Vietnamese Genetic Variation Database	NC_000018.9 - 67508929	Jul 13, 2019 (153)
139	ALFA	NC_000018.10 - 69841693	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)
rs17800176	Oct 08, 2004 (123)
rs59806395	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
15072653509	NC_000018.10:69841692:T:A	NC_000018.10:69841692:T:A	(self)
ss80890731, ss86012590, ss90843085, ss110795333, ss114596610, ss117930045, ss160635085, ss168462875, ss170203666, ss171955118, ss203453339, ss208224428, ss255771625, ss283054003, ss292101117, ss480811179, ss1697965410, ss1713638916, ss2094897678, ss3643180330	NC_000018.8:65659908:T:C	NC_000018.10:69841692:T:C	(self)
75020380, 41582906, 29379864, 4665794, 18525700, 44434719, 604764, 15975920, 1062601, 19412141, 39374644, 10482938, 83857092, 41582906, 9191572, ss227950400, ss237533119, ss243768987, ss480826800, ss481755174, ss485200383, ss537187158, ss565743442, ss661583960, ss778894143, ss783046192, ss784005065, ss832303977, ss834355304, ss993901980, ss1081631430, ss1361667676, ss1428273896, ss1578476793, ss1637224443, ss1680218476, ss1711489004, ss1752265786, ss1809125691, ss1937370219, ss2029459226, ss2095081701, ss2157966584, ss2629228396, ss2633493896, ss2702562371, ss2710872096, ss2958485380, ss3016789127, ss3352102277, ss3627846322, ss3631469533, ss3633168600, ss3633877616, ss3634713236, ss3635564772, ss3636403762, ss3637316424, ss3638205276, ss3640420544, ss3646524627, ss3652279656, ss3683641616, ss3742691055, ss3745013345, ss3755592307, ss3772510799, ss3825917672, ss3835255123, ss3841247637, ss3887357664, ss3937257325, ss3984134783, ss3985836674, ss3986078090, ss4017806763, ss5225887785, ss5315946146, ss5432452160, ss5661620228, ss5799998592, ss5827770317, ss5953051031, ss5981015508	NC_000018.9:67508928:T:C	NC_000018.10:69841692:T:C	(self)
98514006, 529153523, 1638327, 36831699, 117720183, 277872369, 15072653509, ss2222902543, ss3028559969, ss3650827091, ss3701979976, ss3820849228, ss3846750642, ss3980453698, ss5062326706, ss5305855091, ss5498572598, ss5610988071, ss5783883079, ss5817241888, ss5852127383, ss5874734891	NC_000018.10:69841692:T:C	NC_000018.10:69841692:T:C	(self)
ss14418517, ss21504358	NT_025028.13:15299774:T:C	NC_000018.10:69841692:T:C	(self)
ss4930864, ss24509671, ss44138052, ss65734324, ss75005284, ss96522095, ss119458943, ss120253495, ss136364754, ss137458532, ss173620167	NT_025028.14:15299792:T:C	NC_000018.10:69841692:T:C	(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 rs3744856

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

rs3744856