Name: rs762149
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.

rs762149

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:38053544 (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: G>A / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: G=0.401538 (106283/264690, TOPMED)
G=0.420759 (104747/248948, ALFA)
G=0.409077 (57252/139954, GnomAD) (+ 21 more)
G=0.36318 (28580/78694, PAGE_STUDY)
G=0.13402 (3787/28258, 14KJPN)
G=0.13300 (2229/16760, 8.3KJPN)
G=0.3616 (2316/6404, 1000G_30x)
G=0.3516 (1761/5008, 1000G)
G=0.4804 (2152/4480, Estonian)
G=0.4416 (1702/3854, ALSPAC)
G=0.4342 (1610/3708, TWINSUK)
G=0.3531 (668/1892, HapMap)
G=0.1889 (346/1832, Korea1K)
G=0.463 (462/998, GoNL)
G=0.244 (193/790, PRJEB37584)
G=0.318 (191/600, NorthernSweden)
G=0.265 (124/468, SGDP_PRJ)
G=0.310 (67/216, Qatari)
G=0.281 (59/210, Vietnamese)
G=0.25 (11/44, Siberian)
G=0.47 (19/40, GENOME_DK)
G=0.0 (0/8, KOREAN)
C=0.0 (0/8, KOREAN)
T=0.0 (0/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DSCR4 : 500B Downstream 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	253984	G=0.420735	A=0.579265, C=0.000000
European	Sub	224166	G=0.425899	A=0.574101, C=0.000000
African	Sub	8644	G=0.3951	A=0.6049, C=0.0000
African Others	Sub	328	G=0.387	A=0.613, C=0.000
African American	Sub	8316	G=0.3954	A=0.6046, C=0.0000
Asian	Sub	3854	G=0.2390	A=0.7610, C=0.0000
East Asian	Sub	3124	G=0.2020	A=0.7980, C=0.0000
Other Asian	Sub	730	G=0.397	A=0.603, C=0.000
Latin American 1	Sub	1038	G=0.3757	A=0.6243, C=0.0000
Latin American 2	Sub	6600	G=0.4323	A=0.5677, C=0.0000
South Asian	Sub	366	G=0.363	A=0.637, C=0.000
Other	Sub	9316	G=0.3946	A=0.6054, C=0.0000

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	G=0.401538	A=0.598462
Allele Frequency Aggregator	Total	Global	248948	G=0.420759	A=0.579241, C=0.000000
Allele Frequency Aggregator	European	Sub	221072	G=0.425667	A=0.574333, C=0.000000
Allele Frequency Aggregator	Other	Sub	8516	G=0.3955	A=0.6045, C=0.0000
Allele Frequency Aggregator	African	Sub	7502	G=0.3971	A=0.6029, C=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	6600	G=0.4323	A=0.5677, C=0.0000
Allele Frequency Aggregator	Asian	Sub	3854	G=0.2390	A=0.7610, C=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	1038	G=0.3757	A=0.6243, C=0.0000
Allele Frequency Aggregator	South Asian	Sub	366	G=0.363	A=0.637, C=0.000
gnomAD - Genomes	Global	Study-wide	139954	G=0.409077	A=0.590923
gnomAD - Genomes	European	Sub	75836	G=0.43328	A=0.56672
gnomAD - Genomes	African	Sub	41882	G=0.38570	A=0.61430
gnomAD - Genomes	American	Sub	13646	G=0.39447	A=0.60553
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.3414	A=0.6586
gnomAD - Genomes	East Asian	Sub	3122	G=0.2876	A=0.7124
gnomAD - Genomes	Other	Sub	2146	G=0.3844	A=0.6156
The PAGE Study	Global	Study-wide	78694	G=0.36318	A=0.63682
The PAGE Study	AfricanAmerican	Sub	32512	G=0.38810	A=0.61190
The PAGE Study	Mexican	Sub	10810	G=0.42257	A=0.57743
The PAGE Study	Asian	Sub	8316	G=0.1664	A=0.8336
The PAGE Study	PuertoRican	Sub	7918	G=0.3530	A=0.6470
The PAGE Study	NativeHawaiian	Sub	4534	G=0.3191	A=0.6809
The PAGE Study	Cuban	Sub	4230	G=0.3927	A=0.6073
The PAGE Study	Dominican	Sub	3828	G=0.3767	A=0.6233
The PAGE Study	CentralAmerican	Sub	2448	G=0.4167	A=0.5833
The PAGE Study	SouthAmerican	Sub	1982	G=0.4092	A=0.5908
The PAGE Study	NativeAmerican	Sub	1260	G=0.4127	A=0.5873
The PAGE Study	SouthAsian	Sub	856	G=0.367	A=0.633
14KJPN	JAPANESE	Study-wide	28258	G=0.13402	A=0.86598
8.3KJPN	JAPANESE	Study-wide	16760	G=0.13300	A=0.86700
1000Genomes_30x	Global	Study-wide	6404	G=0.3616	A=0.6384
1000Genomes_30x	African	Sub	1786	G=0.3987	A=0.6013
1000Genomes_30x	Europe	Sub	1266	G=0.3768	A=0.6232
1000Genomes_30x	South Asian	Sub	1202	G=0.3694	A=0.6306
1000Genomes_30x	East Asian	Sub	1170	G=0.2410	A=0.7590
1000Genomes_30x	American	Sub	980	G=0.409	A=0.591
1000Genomes	Global	Study-wide	5008	G=0.3516	A=0.6484
1000Genomes	African	Sub	1322	G=0.4002	A=0.5998
1000Genomes	East Asian	Sub	1008	G=0.2252	A=0.7748
1000Genomes	Europe	Sub	1006	G=0.3638	A=0.6362
1000Genomes	South Asian	Sub	978	G=0.368	A=0.632
1000Genomes	American	Sub	694	G=0.402	A=0.598
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.4804	A=0.5196
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.4416	A=0.5584
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.4342	A=0.5658
HapMap	Global	Study-wide	1892	G=0.3531	A=0.6469
HapMap	American	Sub	770	G=0.360	A=0.640
HapMap	African	Sub	692	G=0.429	A=0.571
HapMap	Asian	Sub	254	G=0.161	A=0.839
HapMap	Europe	Sub	176	G=0.301	A=0.699
Korean Genome Project	KOREAN	Study-wide	1832	G=0.1889	A=0.8111
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.463	A=0.537
CNV burdens in cranial meningiomas	Global	Study-wide	790	G=0.244	A=0.756
CNV burdens in cranial meningiomas	CRM	Sub	790	G=0.244	A=0.756
Northern Sweden	ACPOP	Study-wide	600	G=0.318	A=0.682
SGDP_PRJ	Global	Study-wide	468	G=0.265	A=0.735
Qatari	Global	Study-wide	216	G=0.310	A=0.690
A Vietnamese Genetic Variation Database	Global	Study-wide	210	G=0.281	A=0.719
Siberian	Global	Study-wide	44	G=0.25	A=0.75
The Danish reference pan genome	Danish	Study-wide	40	G=0.47	A=0.53
KOREAN population from KRGDB	KOREAN	Study-wide	8	G=0.0	A=1.0, C=0.0, T=0.0

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 21	NC_000021.9:g.38053544G>A
GRCh38.p14 chr 21	NC_000021.9:g.38053544G>C
GRCh38.p14 chr 21	NC_000021.9:g.38053544G>T
GRCh37.p13 chr 21	NC_000021.8:g.39425846G>A
GRCh37.p13 chr 21	NC_000021.8:g.39425846G>C
GRCh37.p13 chr 21	NC_000021.8:g.39425846G>T

Gene: DSCR4, Down syndrome critical region 4 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
DSCR4 transcript	NR_147130.1:n.	N/A	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	G=	A	C	T
GRCh38.p14 chr 21	NC_000021.9:g.38053544=	NC_000021.9:g.38053544G>A	NC_000021.9:g.38053544G>C	NC_000021.9:g.38053544G>T
GRCh37.p13 chr 21	NC_000021.8:g.39425846=	NC_000021.8:g.39425846G>A	NC_000021.8:g.39425846G>C	NC_000021.8:g.39425846G>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#.

120 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss135736	Oct 05, 2000 (86)
2	SC_JCM	ss6271729	Feb 20, 2003 (111)
3	ABI	ss44263233	Mar 13, 2006 (126)
4	ILLUMINA	ss75163636	Dec 07, 2007 (129)
5	HGSV	ss78737640	Dec 07, 2007 (129)
6	BCMHGSC_JDW	ss91837832	Mar 24, 2008 (129)
7	BGI	ss106213555	Feb 03, 2009 (130)
8	1000GENOMES	ss112471065	Jan 25, 2009 (130)
9	1000GENOMES	ss113890728	Jan 25, 2009 (130)
10	ILLUMINA-UK	ss117524783	Feb 14, 2009 (130)
11	KRIBB_YJKIM	ss119366998	Dec 01, 2009 (131)
12	GMI	ss156903774	Dec 01, 2009 (131)
13	ILLUMINA	ss160896277	Dec 01, 2009 (131)
14	COMPLETE_GENOMICS	ss168021574	Jul 04, 2010 (132)
15	COMPLETE_GENOMICS	ss169485677	Jul 04, 2010 (132)
16	COMPLETE_GENOMICS	ss172027231	Jul 04, 2010 (132)
17	ILLUMINA	ss174456505	Jul 04, 2010 (132)
18	BUSHMAN	ss204016937	Jul 04, 2010 (132)
19	BCM-HGSC-SUB	ss208784361	Jul 04, 2010 (132)
20	1000GENOMES	ss228564019	Jul 14, 2010 (132)
21	1000GENOMES	ss237982037	Jul 15, 2010 (132)
22	1000GENOMES	ss244120676	Jul 15, 2010 (132)
23	BL	ss255954452	May 09, 2011 (134)
24	GMI	ss283541668	May 04, 2012 (137)
25	GMI	ss287531043	Apr 25, 2013 (138)
26	PJP	ss292710589	May 09, 2011 (134)
27	ILLUMINA	ss481619903	May 04, 2012 (137)
28	ILLUMINA	ss481650070	May 04, 2012 (137)
29	ILLUMINA	ss482617727	Sep 08, 2015 (146)
30	ILLUMINA	ss485604773	May 04, 2012 (137)
31	ILLUMINA	ss537492078	Sep 08, 2015 (146)
32	TISHKOFF	ss566495776	Apr 25, 2013 (138)
33	SSMP	ss662406244	Apr 25, 2013 (138)
34	ILLUMINA	ss778712232	Sep 08, 2015 (146)
35	ILLUMINA	ss783248000	Sep 08, 2015 (146)
36	ILLUMINA	ss784201662	Sep 08, 2015 (146)
37	ILLUMINA	ss832508676	Sep 08, 2015 (146)
38	ILLUMINA	ss834171413	Sep 08, 2015 (146)
39	EVA-GONL	ss995120132	Aug 21, 2014 (142)
40	JMKIDD_LAB	ss1082500432	Aug 21, 2014 (142)
41	1000GENOMES	ss1366297400	Aug 21, 2014 (142)
42	DDI	ss1429184588	Apr 01, 2015 (144)
43	EVA_GENOME_DK	ss1579663357	Apr 01, 2015 (144)
44	EVA_UK10K_ALSPAC	ss1639565878	Apr 01, 2015 (144)
45	EVA_UK10K_TWINSUK	ss1682559911	Apr 01, 2015 (144)
46	EVA_DECODE	ss1699190533	Apr 01, 2015 (144)
47	EVA_SVP	ss1713723355	Apr 01, 2015 (144)
48	ILLUMINA	ss1752407930	Sep 08, 2015 (146)
49	HAMMER_LAB	ss1809687033	Sep 08, 2015 (146)
50	WEILL_CORNELL_DGM	ss1938670185	Feb 12, 2016 (147)
51	ILLUMINA	ss1946566416	Feb 12, 2016 (147)
52	ILLUMINA	ss1959953292	Feb 12, 2016 (147)
53	GENOMED	ss1969225396	Jul 19, 2016 (147)
54	JJLAB	ss2030107081	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2158711988	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2245794308	Dec 20, 2016 (150)
57	SYSTEMSBIOZJU	ss2629552557	Nov 08, 2017 (151)
58	ILLUMINA	ss2633848747	Nov 08, 2017 (151)
59	ILLUMINA	ss2635109704	Nov 08, 2017 (151)
60	GRF	ss2704442600	Nov 08, 2017 (151)
61	ILLUMINA	ss2710950354	Nov 08, 2017 (151)
62	GNOMAD	ss2971826061	Nov 08, 2017 (151)
63	SWEGEN	ss3018895794	Nov 08, 2017 (151)
64	ILLUMINA	ss3022159385	Nov 08, 2017 (151)
65	BIOINF_KMB_FNS_UNIBA	ss3028892405	Nov 08, 2017 (151)
66	CSHL	ss3352719389	Nov 08, 2017 (151)
67	ILLUMINA	ss3625796730	Oct 12, 2018 (152)
68	ILLUMINA	ss3628481003	Oct 12, 2018 (152)
69	ILLUMINA	ss3631802344	Oct 12, 2018 (152)
70	ILLUMINA	ss3633265151	Oct 12, 2018 (152)
71	ILLUMINA	ss3633980114	Oct 12, 2018 (152)
72	ILLUMINA	ss3634854809	Oct 12, 2018 (152)
73	ILLUMINA	ss3635664848	Oct 12, 2018 (152)
74	ILLUMINA	ss3636550623	Oct 12, 2018 (152)
75	ILLUMINA	ss3637417012	Oct 12, 2018 (152)
76	ILLUMINA	ss3638368067	Oct 12, 2018 (152)
77	ILLUMINA	ss3640562109	Oct 12, 2018 (152)
78	ILLUMINA	ss3643328999	Oct 12, 2018 (152)
79	ILLUMINA	ss3644792649	Oct 12, 2018 (152)
80	ILLUMINA	ss3652619143	Oct 12, 2018 (152)
81	EGCUT_WGS	ss3685472765	Jul 13, 2019 (153)
82	EVA_DECODE	ss3707735883	Jul 13, 2019 (153)
83	ILLUMINA	ss3725947932	Jul 13, 2019 (153)
84	ACPOP	ss3743733859	Jul 13, 2019 (153)
85	ILLUMINA	ss3744203408	Jul 13, 2019 (153)
86	ILLUMINA	ss3745154667	Jul 13, 2019 (153)
87	EVA	ss3759109959	Jul 13, 2019 (153)
88	PAGE_CC	ss3772073923	Jul 13, 2019 (153)
89	ILLUMINA	ss3772650719	Jul 13, 2019 (153)
90	PACBIO	ss3788762940	Jul 13, 2019 (153)
91	PACBIO	ss3793637001	Jul 13, 2019 (153)
92	PACBIO	ss3798523248	Jul 13, 2019 (153)
93	KHV_HUMAN_GENOMES	ss3822276230	Jul 13, 2019 (153)
94	EVA	ss3835874955	Apr 27, 2020 (154)
95	EVA	ss3841564653	Apr 27, 2020 (154)
96	EVA	ss3847078106	Apr 27, 2020 (154)
97	SGDP_PRJ	ss3890006467	Apr 27, 2020 (154)
98	KRGDB	ss3940358792	Apr 27, 2020 (154)
99	KOGIC	ss3983100420	Apr 27, 2020 (154)
100	EVA	ss3984756365	Apr 26, 2021 (155)
101	TOPMED	ss5101716581	Apr 26, 2021 (155)
102	TOMMO_GENOMICS	ss5231544170	Apr 26, 2021 (155)
103	1000G_HIGH_COVERAGE	ss5310227208	Oct 13, 2022 (156)
104	EVA	ss5316038097	Oct 13, 2022 (156)
105	EVA	ss5439905057	Oct 13, 2022 (156)
106	HUGCELL_USP	ss5502273763	Oct 13, 2022 (156)
107	EVA	ss5512324155	Oct 13, 2022 (156)
108	1000G_HIGH_COVERAGE	ss5617374450	Oct 13, 2022 (156)
109	SANFORD_IMAGENETICS	ss5624496577	Oct 13, 2022 (156)
110	SANFORD_IMAGENETICS	ss5664019001	Oct 13, 2022 (156)
111	TOMMO_GENOMICS	ss5792060433	Oct 13, 2022 (156)
112	EVA	ss5800034061	Oct 13, 2022 (156)
113	YY_MCH	ss5818445939	Oct 13, 2022 (156)
114	EVA	ss5839044202	Oct 13, 2022 (156)
115	EVA	ss5847513655	Oct 13, 2022 (156)
116	EVA	ss5847934369	Oct 13, 2022 (156)
117	EVA	ss5853305869	Oct 13, 2022 (156)
118	EVA	ss5892366592	Oct 13, 2022 (156)
119	EVA	ss5958914745	Oct 13, 2022 (156)
120	EVA	ss5979629176	Oct 13, 2022 (156)
121	1000Genomes	NC_000021.8 - 39425846	Oct 12, 2018 (152)
122	1000Genomes_30x	NC_000021.9 - 38053544	Oct 13, 2022 (156)
123	The Avon Longitudinal Study of Parents and Children	NC_000021.8 - 39425846	Oct 12, 2018 (152)
124	Genetic variation in the Estonian population	NC_000021.8 - 39425846	Oct 12, 2018 (152)
125	The Danish reference pan genome	NC_000021.8 - 39425846	Apr 27, 2020 (154)
126	gnomAD - Genomes	NC_000021.9 - 38053544	Apr 26, 2021 (155)
127	Genome of the Netherlands Release 5	NC_000021.8 - 39425846	Apr 27, 2020 (154)
128	HapMap	NC_000021.9 - 38053544	Apr 27, 2020 (154)
129	KOREAN population from KRGDB	NC_000021.8 - 39425846	Apr 27, 2020 (154)
130	Korean Genome Project	NC_000021.9 - 38053544	Apr 27, 2020 (154)
131	Northern Sweden	NC_000021.8 - 39425846	Jul 13, 2019 (153)
132	The PAGE Study	NC_000021.9 - 38053544	Jul 13, 2019 (153)
133	CNV burdens in cranial meningiomas	NC_000021.8 - 39425846	Apr 26, 2021 (155)
134	Qatari	NC_000021.8 - 39425846	Apr 27, 2020 (154)
135	SGDP_PRJ	NC_000021.8 - 39425846	Apr 27, 2020 (154)
136	Siberian	NC_000021.8 - 39425846	Apr 27, 2020 (154)
137	8.3KJPN	NC_000021.8 - 39425846	Apr 26, 2021 (155)
138	14KJPN	NC_000021.9 - 38053544	Oct 13, 2022 (156)
139	TopMed	NC_000021.9 - 38053544	Apr 26, 2021 (155)
140	UK 10K study - Twins	NC_000021.8 - 39425846	Oct 12, 2018 (152)
141	A Vietnamese Genetic Variation Database	NC_000021.8 - 39425846	Jul 13, 2019 (153)
142	ALFA	NC_000021.9 - 38053544	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss78737640, ss91837832, ss112471065, ss113890728, ss117524783, ss168021574, ss169485677, ss172027231, ss204016937, ss208784361, ss255954452, ss283541668, ss287531043, ss292710589, ss481619903, ss1699190533, ss1713723355, ss2635109704, ss3643328999	NC_000021.7:38347715:G:A	NC_000021.9:38053543:G:A	(self)
79817651, 44174018, 31211013, 5828296, 19677901, 47536186, 17018724, 305944, 20712107, 42023447, 11228342, 89513477, 44174018, 9746438, ss228564019, ss237982037, ss244120676, ss481650070, ss482617727, ss485604773, ss537492078, ss566495776, ss662406244, ss778712232, ss783248000, ss784201662, ss832508676, ss834171413, ss995120132, ss1082500432, ss1366297400, ss1429184588, ss1579663357, ss1639565878, ss1682559911, ss1752407930, ss1809687033, ss1938670185, ss1946566416, ss1959953292, ss1969225396, ss2030107081, ss2158711988, ss2629552557, ss2633848747, ss2704442600, ss2710950354, ss2971826061, ss3018895794, ss3022159385, ss3352719389, ss3625796730, ss3628481003, ss3631802344, ss3633265151, ss3633980114, ss3634854809, ss3635664848, ss3636550623, ss3637417012, ss3638368067, ss3640562109, ss3644792649, ss3652619143, ss3685472765, ss3743733859, ss3744203408, ss3745154667, ss3759109959, ss3772650719, ss3788762940, ss3793637001, ss3798523248, ss3835874955, ss3841564653, ss3890006467, ss3940358792, ss3984756365, ss5231544170, ss5316038097, ss5439905057, ss5512324155, ss5624496577, ss5664019001, ss5800034061, ss5839044202, ss5847513655, ss5847934369, ss5958914745, ss5979629176	NC_000021.8:39425845:G:A	NC_000021.9:38053543:G:A	(self)
104900385, 563272546, 2209541, 39478421, 1295392, 125897537, 376825527, 9843997548, ss2245794308, ss3028892405, ss3707735883, ss3725947932, ss3772073923, ss3822276230, ss3847078106, ss3983100420, ss5101716581, ss5310227208, ss5502273763, ss5617374450, ss5792060433, ss5818445939, ss5853305869, ss5892366592	NC_000021.9:38053543:G:A	NC_000021.9:38053543:G:A	(self)
ss135736, ss6271729, ss44263233, ss75163636, ss106213555, ss119366998, ss156903774, ss160896277, ss174456505	NT_011512.11:25087716:G:A	NC_000021.9:38053543:G:A	(self)
47536186, ss3940358792	NC_000021.8:39425845:G:C	NC_000021.9:38053543:G:C	(self)
9843997548	NC_000021.9:38053543:G:C	NC_000021.9:38053543:G:C	(self)
47536186, ss3940358792	NC_000021.8:39425845:G:T	NC_000021.9:38053543:G: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 rs762149

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

rs762149