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dbSNP Short Genetic Variations

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.

rs62127952

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr19:49185599 (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
T=0.116219 (30762/264690, TOPMED)
T=0.133902 (18723/139826, GnomAD)
T=0.06737 (5302/78700, PAGE_STUDY) (+ 17 more)
T=0.13130 (3774/28744, ALFA)
T=0.01872 (529/28258, 14KJPN)
T=0.01844 (309/16760, 8.3KJPN)
T=0.0849 (544/6404, 1000G_30x)
T=0.0857 (429/5008, 1000G)
T=0.2292 (1027/4480, Estonian)
T=0.1814 (699/3854, ALSPAC)
T=0.1750 (649/3708, TWINSUK)
T=0.0202 (59/2922, KOREAN)
T=0.195 (195/998, GoNL)
T=0.248 (149/600, NorthernSweden)
T=0.102 (22/216, Qatari)
T=0.056 (12/214, Vietnamese)
C=0.48 (40/84, SGDP_PRJ)
T=0.15 (6/40, GENOME_DK)
T=0.40 (8/20, Ancient Sardinia)
C=0.43 (6/14, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
TRPM4 : 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 28744 C=0.86870 G=0.00000, T=0.13130
European Sub 22504 C=0.84554 G=0.00000, T=0.15446
African Sub 3444 C=0.9878 G=0.0000, T=0.0122
African Others Sub 124 C=1.000 G=0.000, T=0.000
African American Sub 3320 C=0.9873 G=0.0000, T=0.0127
Asian Sub 144 C=0.993 G=0.000, T=0.007
East Asian Sub 126 C=0.992 G=0.000, T=0.008
Other Asian Sub 18 C=1.00 G=0.00, T=0.00
Latin American 1 Sub 136 C=0.985 G=0.000, T=0.015
Latin American 2 Sub 584 C=0.986 G=0.000, T=0.014
South Asian Sub 106 C=0.981 G=0.000, T=0.019
Other Sub 1826 C=0.8669 G=0.0000, T=0.1331


Help

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 C=0.883781 T=0.116219
gnomAD - Genomes Global Study-wide 139826 C=0.866098 T=0.133902
gnomAD - Genomes European Sub 75760 C=0.80347 T=0.19653
gnomAD - Genomes African Sub 41888 C=0.96505 T=0.03495
gnomAD - Genomes American Sub 13592 C=0.89553 T=0.10447
gnomAD - Genomes Ashkenazi Jewish Sub 3322 C=0.8525 T=0.1475
gnomAD - Genomes East Asian Sub 3120 C=0.9471 T=0.0529
gnomAD - Genomes Other Sub 2144 C=0.8624 T=0.1376
The PAGE Study Global Study-wide 78700 C=0.93263 T=0.06737
The PAGE Study AfricanAmerican Sub 32516 C=0.95999 T=0.04001
The PAGE Study Mexican Sub 10808 C=0.91506 T=0.08494
The PAGE Study Asian Sub 8318 C=0.9756 T=0.0244
The PAGE Study PuertoRican Sub 7918 C=0.8879 T=0.1121
The PAGE Study NativeHawaiian Sub 4534 C=0.8963 T=0.1037
The PAGE Study Cuban Sub 4230 C=0.8506 T=0.1494
The PAGE Study Dominican Sub 3828 C=0.9237 T=0.0763
The PAGE Study CentralAmerican Sub 2450 C=0.9286 T=0.0714
The PAGE Study SouthAmerican Sub 1982 C=0.9132 T=0.0868
The PAGE Study NativeAmerican Sub 1260 C=0.8690 T=0.1310
The PAGE Study SouthAsian Sub 856 C=0.900 T=0.100
Allele Frequency Aggregator Total Global 28744 C=0.86870 G=0.00000, T=0.13130
Allele Frequency Aggregator European Sub 22504 C=0.84554 G=0.00000, T=0.15446
Allele Frequency Aggregator African Sub 3444 C=0.9878 G=0.0000, T=0.0122
Allele Frequency Aggregator Other Sub 1826 C=0.8669 G=0.0000, T=0.1331
Allele Frequency Aggregator Latin American 2 Sub 584 C=0.986 G=0.000, T=0.014
Allele Frequency Aggregator Asian Sub 144 C=0.993 G=0.000, T=0.007
Allele Frequency Aggregator Latin American 1 Sub 136 C=0.985 G=0.000, T=0.015
Allele Frequency Aggregator South Asian Sub 106 C=0.981 G=0.000, T=0.019
14KJPN JAPANESE Study-wide 28258 C=0.98128 T=0.01872
8.3KJPN JAPANESE Study-wide 16760 C=0.98156 T=0.01844
1000Genomes_30x Global Study-wide 6404 C=0.9151 T=0.0849
1000Genomes_30x African Sub 1786 C=0.9849 T=0.0151
1000Genomes_30x Europe Sub 1266 C=0.7923 T=0.2077
1000Genomes_30x South Asian Sub 1202 C=0.9035 T=0.0965
1000Genomes_30x East Asian Sub 1170 C=0.9547 T=0.0453
1000Genomes_30x American Sub 980 C=0.913 T=0.087
1000Genomes Global Study-wide 5008 C=0.9143 T=0.0857
1000Genomes African Sub 1322 C=0.9879 T=0.0121
1000Genomes East Asian Sub 1008 C=0.9563 T=0.0437
1000Genomes Europe Sub 1006 C=0.7893 T=0.2107
1000Genomes South Asian Sub 978 C=0.906 T=0.094
1000Genomes American Sub 694 C=0.906 T=0.094
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.7708 T=0.2292
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.8186 T=0.1814
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.8250 T=0.1750
KOREAN population from KRGDB KOREAN Study-wide 2922 C=0.9798 T=0.0202
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.805 T=0.195
Northern Sweden ACPOP Study-wide 600 C=0.752 T=0.248
Qatari Global Study-wide 216 C=0.898 T=0.102
A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.944 T=0.056
SGDP_PRJ Global Study-wide 84 C=0.48 T=0.52
The Danish reference pan genome Danish Study-wide 40 C=0.85 T=0.15
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 20 C=0.60 T=0.40
Siberian Global Study-wide 14 C=0.43 T=0.57
Help

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 19 NC_000019.10:g.49185599C>G
GRCh38.p14 chr 19 NC_000019.10:g.49185599C>T
GRCh37.p13 chr 19 NC_000019.9:g.49688856C>G
GRCh37.p13 chr 19 NC_000019.9:g.49688856C>T
TRPM4 RefSeqGene NG_027551.2:g.32841C>G
TRPM4 RefSeqGene NG_027551.2:g.32841C>T
Gene: TRPM4, transient receptor potential cation channel subfamily M member 4 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TRPM4 transcript variant 2 NM_001195227.2:c.1743+238…

NM_001195227.2:c.1743+2387C>G

N/A Intron Variant
TRPM4 transcript variant 3 NM_001321281.2:c.1398+238…

NM_001321281.2:c.1398+2387C>G

N/A Intron Variant
TRPM4 transcript variant 4 NM_001321282.2:c.135+2387…

NM_001321282.2:c.135+2387C>G

N/A Intron Variant
TRPM4 transcript variant 5 NM_001321283.2:c.1221+238…

NM_001321283.2:c.1221+2387C>G

N/A Intron Variant
TRPM4 transcript variant 6 NM_001321285.2:c.681+2387…

NM_001321285.2:c.681+2387C>G

N/A Intron Variant
TRPM4 transcript variant 1 NM_017636.4:c.1743+2387C>G N/A Intron Variant
TRPM4 transcript variant X1 XM_047438992.1:c.2214+238…

XM_047438992.1:c.2214+2387C>G

N/A Intron Variant
TRPM4 transcript variant X2 XM_047438993.1:c.456+2387…

XM_047438993.1:c.456+2387C>G

N/A Intron Variant
Help

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
Help

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 19 NC_000019.10:g.49185599= NC_000019.10:g.49185599C>G NC_000019.10:g.49185599C>T
GRCh37.p13 chr 19 NC_000019.9:g.49688856= NC_000019.9:g.49688856C>G NC_000019.9:g.49688856C>T
TRPM4 RefSeqGene NG_027551.2:g.32841= NG_027551.2:g.32841C>G NG_027551.2:g.32841C>T
TRPM4 transcript variant 2 NM_001195227.1:c.1743+2387= NM_001195227.1:c.1743+2387C>G NM_001195227.1:c.1743+2387C>T
TRPM4 transcript variant 2 NM_001195227.2:c.1743+2387= NM_001195227.2:c.1743+2387C>G NM_001195227.2:c.1743+2387C>T
TRPM4 transcript variant 3 NM_001321281.2:c.1398+2387= NM_001321281.2:c.1398+2387C>G NM_001321281.2:c.1398+2387C>T
TRPM4 transcript variant 4 NM_001321282.2:c.135+2387= NM_001321282.2:c.135+2387C>G NM_001321282.2:c.135+2387C>T
TRPM4 transcript variant 5 NM_001321283.2:c.1221+2387= NM_001321283.2:c.1221+2387C>G NM_001321283.2:c.1221+2387C>T
TRPM4 transcript variant 6 NM_001321285.2:c.681+2387= NM_001321285.2:c.681+2387C>G NM_001321285.2:c.681+2387C>T
TRPM4 transcript variant 1 NM_017636.3:c.1743+2387= NM_017636.3:c.1743+2387C>G NM_017636.3:c.1743+2387C>T
TRPM4 transcript variant 1 NM_017636.4:c.1743+2387= NM_017636.4:c.1743+2387C>G NM_017636.4:c.1743+2387C>T
TRPM4 transcript variant X1 XM_005259015.1:c.1221+2387= XM_005259015.1:c.1221+2387C>G XM_005259015.1:c.1221+2387C>T
TRPM4 transcript variant X2 XM_005259016.1:c.681+2387= XM_005259016.1:c.681+2387C>G XM_005259016.1:c.681+2387C>T
TRPM4 transcript variant X1 XM_005259017.1:c.456+2387= XM_005259017.1:c.456+2387C>G XM_005259017.1:c.456+2387C>T
TRPM4 transcript variant X4 XM_005259018.1:c.135+2387= XM_005259018.1:c.135+2387C>G XM_005259018.1:c.135+2387C>T
TRPM4 transcript variant X1 XM_047438992.1:c.2214+2387= XM_047438992.1:c.2214+2387C>G XM_047438992.1:c.2214+2387C>T
TRPM4 transcript variant X2 XM_047438993.1:c.456+2387= XM_047438993.1:c.456+2387C>G XM_047438993.1:c.456+2387C>T
Help

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#.

73 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCMHGSC_JDW ss90995934 Mar 24, 2008 (129)
2 1000GENOMES ss111465943 Jan 25, 2009 (130)
3 ENSEMBL ss137710597 Dec 01, 2009 (131)
4 COMPLETE_GENOMICS ss168295102 Jul 04, 2010 (132)
5 COMPLETE_GENOMICS ss171813743 Jul 04, 2010 (132)
6 1000GENOMES ss237699846 Jul 15, 2010 (132)
7 GMI ss287393646 Apr 25, 2013 (138)
8 ILLUMINA ss483840935 May 04, 2012 (137)
9 ILLUMINA ss484230867 May 04, 2012 (137)
10 ILLUMINA ss536417140 Sep 08, 2015 (146)
11 SSMP ss661895071 Apr 25, 2013 (138)
12 ILLUMINA ss779529169 Sep 08, 2015 (146)
13 ILLUMINA ss782561416 Sep 08, 2015 (146)
14 ILLUMINA ss834999714 Sep 08, 2015 (146)
15 EVA-GONL ss994372368 Aug 21, 2014 (142)
16 JMKIDD_LAB ss1081952400 Aug 21, 2014 (142)
17 1000GENOMES ss1363457270 Aug 21, 2014 (142)
18 DDI ss1428423242 Apr 01, 2015 (144)
19 EVA_GENOME_DK ss1578666883 Apr 01, 2015 (144)
20 EVA_UK10K_ALSPAC ss1638103515 Apr 01, 2015 (144)
21 EVA_UK10K_TWINSUK ss1681097548 Apr 01, 2015 (144)
22 EVA_DECODE ss1698427359 Apr 01, 2015 (144)
23 WEILL_CORNELL_DGM ss1937872358 Feb 12, 2016 (147)
24 ILLUMINA ss1959874862 Feb 12, 2016 (147)
25 GENOMED ss1968655897 Jul 19, 2016 (147)
26 JJLAB ss2029711701 Sep 14, 2016 (149)
27 USC_VALOUEV ss2158259085 Dec 20, 2016 (150)
28 HUMAN_LONGEVITY ss2226274389 Dec 20, 2016 (150)
29 ILLUMINA ss2633548348 Nov 08, 2017 (151)
30 GRF ss2702872020 Nov 08, 2017 (151)
31 GNOMAD ss2963721777 Nov 08, 2017 (151)
32 SWEGEN ss3017600563 Nov 08, 2017 (151)
33 ILLUMINA ss3021916827 Nov 08, 2017 (151)
34 BIOINF_KMB_FNS_UNIBA ss3028686454 Nov 08, 2017 (151)
35 CSHL ss3352336787 Nov 08, 2017 (151)
36 ILLUMINA ss3627949833 Oct 12, 2018 (152)
37 ILLUMINA ss3631518951 Oct 12, 2018 (152)
38 ILLUMINA ss3652343521 Oct 12, 2018 (152)
39 EGCUT_WGS ss3684339361 Jul 13, 2019 (153)
40 EVA_DECODE ss3702914990 Jul 13, 2019 (153)
41 ILLUMINA ss3725737850 Jul 13, 2019 (153)
42 ACPOP ss3743102653 Jul 13, 2019 (153)
43 EVA ss3756149792 Jul 13, 2019 (153)
44 PAGE_CC ss3772020489 Jul 13, 2019 (153)
45 PACBIO ss3788551748 Jul 13, 2019 (153)
46 PACBIO ss3793458229 Jul 13, 2019 (153)
47 PACBIO ss3798345111 Jul 13, 2019 (153)
48 KHV_HUMAN_GENOMES ss3821399002 Jul 13, 2019 (153)
49 EVA ss3835499026 Apr 27, 2020 (154)
50 EVA ss3841372281 Apr 27, 2020 (154)
51 EVA ss3846878614 Apr 27, 2020 (154)
52 SGDP_PRJ ss3888380155 Apr 27, 2020 (154)
53 KRGDB ss3938526357 Apr 27, 2020 (154)
54 EVA ss3985857683 Apr 26, 2021 (155)
55 TOPMED ss5077263653 Apr 26, 2021 (155)
56 TOMMO_GENOMICS ss5228119235 Apr 26, 2021 (155)
57 EVA ss5237598504 Apr 26, 2021 (155)
58 1000G_HIGH_COVERAGE ss5307522929 Oct 13, 2022 (156)
59 EVA ss5315979737 Oct 13, 2022 (156)
60 EVA ss5435298848 Oct 13, 2022 (156)
61 HUGCELL_USP ss5499998395 Oct 13, 2022 (156)
62 1000G_HIGH_COVERAGE ss5613367275 Oct 13, 2022 (156)
63 SANFORD_IMAGENETICS ss5624430746 Oct 13, 2022 (156)
64 SANFORD_IMAGENETICS ss5662543598 Oct 13, 2022 (156)
65 TOMMO_GENOMICS ss5786875172 Oct 13, 2022 (156)
66 YY_MCH ss5817666547 Oct 13, 2022 (156)
67 EVA ss5840653992 Oct 13, 2022 (156)
68 EVA ss5847498414 Oct 13, 2022 (156)
69 EVA ss5852316597 Oct 13, 2022 (156)
70 EVA ss5928386514 Oct 13, 2022 (156)
71 EVA ss5953949875 Oct 13, 2022 (156)
72 EVA ss5979549257 Oct 13, 2022 (156)
73 EVA ss5981061509 Oct 13, 2022 (156)
74 1000Genomes NC_000019.9 - 49688856 Oct 12, 2018 (152)
75 1000Genomes_30x NC_000019.10 - 49185599 Oct 13, 2022 (156)
76 The Avon Longitudinal Study of Parents and Children NC_000019.9 - 49688856 Oct 12, 2018 (152)
77 Genetic variation in the Estonian population NC_000019.9 - 49688856 Oct 12, 2018 (152)
78 The Danish reference pan genome NC_000019.9 - 49688856 Apr 27, 2020 (154)
79 gnomAD - Genomes NC_000019.10 - 49185599 Apr 26, 2021 (155)
80 Genome of the Netherlands Release 5 NC_000019.9 - 49688856 Apr 27, 2020 (154)
81 KOREAN population from KRGDB NC_000019.9 - 49688856 Apr 27, 2020 (154)
82 Northern Sweden NC_000019.9 - 49688856 Jul 13, 2019 (153)
83 The PAGE Study NC_000019.10 - 49185599 Jul 13, 2019 (153)
84 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000019.9 - 49688856 Apr 26, 2021 (155)
85 Qatari NC_000019.9 - 49688856 Apr 27, 2020 (154)
86 SGDP_PRJ NC_000019.9 - 49688856 Apr 27, 2020 (154)
87 Siberian NC_000019.9 - 49688856 Apr 27, 2020 (154)
88 8.3KJPN NC_000019.9 - 49688856 Apr 26, 2021 (155)
89 14KJPN NC_000019.10 - 49185599 Oct 13, 2022 (156)
90 TopMed NC_000019.10 - 49185599 Apr 26, 2021 (155)
91 UK 10K study - Twins NC_000019.9 - 49688856 Oct 12, 2018 (152)
92 A Vietnamese Genetic Variation Database NC_000019.9 - 49688856 Jul 13, 2019 (153)
93 ALFA NC_000019.10 - 49185599 Apr 26, 2021 (155)
Help

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
10226934329 NC_000019.10:49185598:C:G NC_000019.10:49185598:C:G (self)
ss90995934, ss111465943, ss168295102, ss171813743, ss287393646, ss483840935, ss1698427359 NC_000019.8:54380667:C:T NC_000019.10:49185598:C:T (self)
76874924, 42561817, 30077609, 4848316, 18960370, 45703751, 16387518, 1083610, 19914280, 40397135, 10775439, 86088542, 42561817, 9396789, ss237699846, ss484230867, ss536417140, ss661895071, ss779529169, ss782561416, ss834999714, ss994372368, ss1081952400, ss1363457270, ss1428423242, ss1578666883, ss1638103515, ss1681097548, ss1937872358, ss1959874862, ss1968655897, ss2029711701, ss2158259085, ss2633548348, ss2702872020, ss2963721777, ss3017600563, ss3021916827, ss3352336787, ss3627949833, ss3631518951, ss3652343521, ss3684339361, ss3743102653, ss3756149792, ss3788551748, ss3793458229, ss3798345111, ss3835499026, ss3841372281, ss3888380155, ss3938526357, ss3985857683, ss5228119235, ss5237598504, ss5315979737, ss5435298848, ss5624430746, ss5662543598, ss5840653992, ss5847498414, ss5953949875, ss5979549257, ss5981061509 NC_000019.9:49688855:C:T NC_000019.10:49185598:C:T (self)
100893210, 542170313, 1241958, 120712276, 292809317, 10226934329, ss2226274389, ss3028686454, ss3702914990, ss3725737850, ss3772020489, ss3821399002, ss3846878614, ss5077263653, ss5307522929, ss5499998395, ss5613367275, ss5786875172, ss5817666547, ss5852316597, ss5928386514 NC_000019.10:49185598:C:T NC_000019.10:49185598:C:T (self)
ss137710597 NT_011109.16:21957073:C:T NC_000019.10:49185598:C:T (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs62127952

Help

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.

Software version is: 2.0.1.post761+d5e8e07