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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.

rs3738196

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:164768956 (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>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.479070 (126805/264690, TOPMED)
G=0.498225 (69606/139708, GnomAD)
G=0.42108 (11898/28256, 14KJPN) (+ 16 more)
T=0.46537 (8789/18886, ALFA)
G=0.42184 (7070/16760, 8.3KJPN)
G=0.4074 (2609/6404, 1000G_30x)
G=0.4089 (2048/5008, 1000G)
T=0.4540 (2032/4476, Estonian)
T=0.3594 (1385/3854, ALSPAC)
T=0.3711 (1376/3708, TWINSUK)
G=0.3959 (1160/2930, KOREAN)
G=0.4361 (799/1832, Korea1K)
T=0.370 (369/998, GoNL)
T=0.368 (221/600, NorthernSweden)
T=0.363 (124/342, SGDP_PRJ)
T=0.468 (101/216, Qatari)
G=0.381 (80/210, Vietnamese)
T=0.30 (13/44, Siberian)
T=0.28 (11/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PBX1 : Intron Variant
PBX1-AS1 : 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 18886 T=0.46537 G=0.53463
European Sub 14282 T=0.40365 G=0.59635
African Sub 2946 T=0.7138 G=0.2862
African Others Sub 114 T=0.772 G=0.228
African American Sub 2832 T=0.7115 G=0.2885
Asian Sub 112 T=0.580 G=0.420
East Asian Sub 86 T=0.57 G=0.43
Other Asian Sub 26 T=0.62 G=0.38
Latin American 1 Sub 146 T=0.445 G=0.555
Latin American 2 Sub 610 T=0.602 G=0.398
South Asian Sub 98 T=0.46 G=0.54
Other Sub 692 T=0.548 G=0.452


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 T=0.520930 G=0.479070
gnomAD - Genomes Global Study-wide 139708 T=0.501775 G=0.498225
gnomAD - Genomes European Sub 75744 T=0.37938 G=0.62062
gnomAD - Genomes African Sub 41778 T=0.70870 G=0.29130
gnomAD - Genomes American Sub 13614 T=0.54003 G=0.45997
gnomAD - Genomes Ashkenazi Jewish Sub 3318 T=0.4521 G=0.5479
gnomAD - Genomes East Asian Sub 3112 T=0.5964 G=0.4036
gnomAD - Genomes Other Sub 2142 T=0.4902 G=0.5098
14KJPN JAPANESE Study-wide 28256 T=0.57892 G=0.42108
Allele Frequency Aggregator Total Global 18886 T=0.46537 G=0.53463
Allele Frequency Aggregator European Sub 14282 T=0.40365 G=0.59635
Allele Frequency Aggregator African Sub 2946 T=0.7138 G=0.2862
Allele Frequency Aggregator Other Sub 692 T=0.548 G=0.452
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.602 G=0.398
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.445 G=0.555
Allele Frequency Aggregator Asian Sub 112 T=0.580 G=0.420
Allele Frequency Aggregator South Asian Sub 98 T=0.46 G=0.54
8.3KJPN JAPANESE Study-wide 16760 T=0.57816 G=0.42184
1000Genomes_30x Global Study-wide 6404 T=0.5926 G=0.4074
1000Genomes_30x African Sub 1786 T=0.7732 G=0.2268
1000Genomes_30x Europe Sub 1266 T=0.3957 G=0.6043
1000Genomes_30x South Asian Sub 1202 T=0.5624 G=0.4376
1000Genomes_30x East Asian Sub 1170 T=0.5761 G=0.4239
1000Genomes_30x American Sub 980 T=0.574 G=0.426
1000Genomes Global Study-wide 5008 T=0.5911 G=0.4089
1000Genomes African Sub 1322 T=0.7738 G=0.2262
1000Genomes East Asian Sub 1008 T=0.5863 G=0.4137
1000Genomes Europe Sub 1006 T=0.3907 G=0.6093
1000Genomes South Asian Sub 978 T=0.562 G=0.438
1000Genomes American Sub 694 T=0.581 G=0.419
Genetic variation in the Estonian population Estonian Study-wide 4476 T=0.4540 G=0.5460
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.3594 G=0.6406
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.3711 G=0.6289
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.6041 C=0.0000, G=0.3959
Korean Genome Project KOREAN Study-wide 1832 T=0.5639 G=0.4361
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.370 G=0.630
Northern Sweden ACPOP Study-wide 600 T=0.368 G=0.632
SGDP_PRJ Global Study-wide 342 T=0.363 G=0.637
Qatari Global Study-wide 216 T=0.468 G=0.532
A Vietnamese Genetic Variation Database Global Study-wide 210 T=0.619 G=0.381
Siberian Global Study-wide 44 T=0.30 G=0.70
The Danish reference pan genome Danish Study-wide 40 T=0.28 G=0.72
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 1 NC_000001.11:g.164768956T>C
GRCh38.p14 chr 1 NC_000001.11:g.164768956T>G
GRCh37.p13 chr 1 NC_000001.10:g.164738193T>C
GRCh37.p13 chr 1 NC_000001.10:g.164738193T>G
PBX1 RefSeqGene NG_028246.2:g.214597T>C
PBX1 RefSeqGene NG_028246.2:g.214597T>G
Gene: PBX1, PBX homeobox 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PBX1 transcript variant 2 NM_001204961.2:c.266-2353…

NM_001204961.2:c.266-23538T>C

N/A Intron Variant
PBX1 transcript variant 3 NM_001204963.2:c.266-2353…

NM_001204963.2:c.266-23538T>C

N/A Intron Variant
PBX1 transcript variant 4 NM_001353130.1:c.17-23538…

NM_001353130.1:c.17-23538T>C

N/A Intron Variant
PBX1 transcript variant 5 NM_001353131.2:c.266-2353…

NM_001353131.2:c.266-23538T>C

N/A Intron Variant
PBX1 transcript variant 1 NM_002585.4:c.266-23538T>C N/A Intron Variant
PBX1 transcript variant X3 XM_005245229.4:c.266-2353…

XM_005245229.4:c.266-23538T>C

N/A Intron Variant
PBX1 transcript variant X2 XM_011509590.3:c.434-2353…

XM_011509590.3:c.434-23538T>C

N/A Intron Variant
PBX1 transcript variant X5 XM_011509592.3:c.434-2353…

XM_011509592.3:c.434-23538T>C

N/A Intron Variant
PBX1 transcript variant X4 XM_017001395.3:c.266-2353…

XM_017001395.3:c.266-23538T>C

N/A Intron Variant
PBX1 transcript variant X1 XM_047421783.1:c.434-2353…

XM_047421783.1:c.434-23538T>C

N/A Intron Variant
PBX1 transcript variant X6 XM_047421784.1:c.266-2353…

XM_047421784.1:c.266-23538T>C

N/A Intron Variant
PBX1 transcript variant X7 XM_047421787.1:c. N/A Genic Downstream Transcript Variant
Gene: PBX1-AS1, PBX1 antisense RNA 1 (minus strand) : 500B Downstream Variant
Molecule type Change Amino acid[Codon] SO Term
PBX1-AS1 transcript NR_038072.1:n. N/A Downstream Transcript 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 T= C G
GRCh38.p14 chr 1 NC_000001.11:g.164768956= NC_000001.11:g.164768956T>C NC_000001.11:g.164768956T>G
GRCh37.p13 chr 1 NC_000001.10:g.164738193= NC_000001.10:g.164738193T>C NC_000001.10:g.164738193T>G
PBX1 RefSeqGene NG_028246.2:g.214597= NG_028246.2:g.214597T>C NG_028246.2:g.214597T>G
PBX1 transcript variant 2 NM_001204961.1:c.266-23538= NM_001204961.1:c.266-23538T>C NM_001204961.1:c.266-23538T>G
PBX1 transcript variant 2 NM_001204961.2:c.266-23538= NM_001204961.2:c.266-23538T>C NM_001204961.2:c.266-23538T>G
PBX1 transcript variant 3 NM_001204963.1:c.266-23538= NM_001204963.1:c.266-23538T>C NM_001204963.1:c.266-23538T>G
PBX1 transcript variant 3 NM_001204963.2:c.266-23538= NM_001204963.2:c.266-23538T>C NM_001204963.2:c.266-23538T>G
PBX1 transcript variant 4 NM_001353130.1:c.17-23538= NM_001353130.1:c.17-23538T>C NM_001353130.1:c.17-23538T>G
PBX1 transcript variant 5 NM_001353131.2:c.266-23538= NM_001353131.2:c.266-23538T>C NM_001353131.2:c.266-23538T>G
PBX1 transcript variant 1 NM_002585.3:c.266-23538= NM_002585.3:c.266-23538T>C NM_002585.3:c.266-23538T>G
PBX1 transcript variant 1 NM_002585.4:c.266-23538= NM_002585.4:c.266-23538T>C NM_002585.4:c.266-23538T>G
PBX1 transcript variant X1 XM_005245228.1:c.434-23538= XM_005245228.1:c.434-23538T>C XM_005245228.1:c.434-23538T>G
PBX1 transcript variant X2 XM_005245229.1:c.266-23538= XM_005245229.1:c.266-23538T>C XM_005245229.1:c.266-23538T>G
PBX1 transcript variant X3 XM_005245229.4:c.266-23538= XM_005245229.4:c.266-23538T>C XM_005245229.4:c.266-23538T>G
PBX1 transcript variant X3 XM_005245230.1:c.-50-23538= XM_005245230.1:c.-50-23538T>C XM_005245230.1:c.-50-23538T>G
PBX1 transcript variant X2 XM_011509590.3:c.434-23538= XM_011509590.3:c.434-23538T>C XM_011509590.3:c.434-23538T>G
PBX1 transcript variant X5 XM_011509592.3:c.434-23538= XM_011509592.3:c.434-23538T>C XM_011509592.3:c.434-23538T>G
PBX1 transcript variant X4 XM_017001395.3:c.266-23538= XM_017001395.3:c.266-23538T>C XM_017001395.3:c.266-23538T>G
PBX1 transcript variant X1 XM_047421783.1:c.434-23538= XM_047421783.1:c.434-23538T>C XM_047421783.1:c.434-23538T>G
PBX1 transcript variant X6 XM_047421784.1:c.266-23538= XM_047421784.1:c.266-23538T>C XM_047421784.1:c.266-23538T>G
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#.

74 SubSNP, 19 Frequency submissions
No Submitter Submission ID Date (Build)
1 YUSUKE ss4924195 Aug 28, 2002 (107)
2 SC_SNP ss18339051 Feb 28, 2004 (126)
3 HGSV ss77512032 Dec 07, 2007 (129)
4 HGSV ss85561820 Dec 15, 2007 (130)
5 BCMHGSC_JDW ss87850267 Mar 23, 2008 (129)
6 HUMANGENOME_JCVI ss99256772 Feb 06, 2009 (130)
7 BGI ss102792339 Dec 01, 2009 (131)
8 1000GENOMES ss111263994 Jan 25, 2009 (130)
9 ENSEMBL ss138095139 Dec 01, 2009 (131)
10 ENSEMBL ss142633214 Dec 01, 2009 (131)
11 GMI ss155852840 Dec 01, 2009 (131)
12 COMPLETE_GENOMICS ss164288003 Jul 04, 2010 (132)
13 COMPLETE_GENOMICS ss167216796 Jul 04, 2010 (132)
14 BUSHMAN ss199174478 Jul 04, 2010 (132)
15 BCM-HGSC-SUB ss205343911 Jul 04, 2010 (132)
16 1000GENOMES ss210465441 Jul 14, 2010 (132)
17 1000GENOMES ss218688155 Jul 14, 2010 (132)
18 1000GENOMES ss230759529 Jul 14, 2010 (132)
19 1000GENOMES ss238402192 Jul 15, 2010 (132)
20 BL ss253562780 May 09, 2011 (134)
21 GMI ss276080652 May 04, 2012 (137)
22 PJP ss290652057 May 09, 2011 (134)
23 TISHKOFF ss554789310 Apr 25, 2013 (138)
24 SSMP ss648463059 Apr 25, 2013 (138)
25 EVA-GONL ss975757611 Aug 21, 2014 (142)
26 JMKIDD_LAB ss1068323152 Aug 21, 2014 (142)
27 1000GENOMES ss1293210974 Aug 21, 2014 (142)
28 DDI ss1426000996 Apr 01, 2015 (144)
29 EVA_GENOME_DK ss1574441326 Apr 01, 2015 (144)
30 EVA_DECODE ss1585141688 Apr 01, 2015 (144)
31 EVA_UK10K_ALSPAC ss1601364730 Apr 01, 2015 (144)
32 EVA_UK10K_TWINSUK ss1644358763 Apr 01, 2015 (144)
33 HAMMER_LAB ss1795190661 Sep 08, 2015 (146)
34 WEILL_CORNELL_DGM ss1918993777 Feb 12, 2016 (147)
35 GENOMED ss1966884620 Jul 19, 2016 (147)
36 JJLAB ss2020011851 Sep 14, 2016 (149)
37 USC_VALOUEV ss2148038834 Dec 20, 2016 (150)
38 HUMAN_LONGEVITY ss2167109492 Dec 20, 2016 (150)
39 SYSTEMSBIOZJU ss2624514977 Nov 08, 2017 (151)
40 GRF ss2698015683 Nov 08, 2017 (151)
41 GNOMAD ss2762127656 Nov 08, 2017 (151)
42 AFFY ss2985528580 Nov 08, 2017 (151)
43 SWEGEN ss2987869373 Nov 08, 2017 (151)
44 BIOINF_KMB_FNS_UNIBA ss3023763351 Nov 08, 2017 (151)
45 CSHL ss3343744009 Nov 08, 2017 (151)
46 URBANLAB ss3646807326 Oct 11, 2018 (152)
47 EGCUT_WGS ss3655809903 Jul 12, 2019 (153)
48 EVA_DECODE ss3687922706 Jul 12, 2019 (153)
49 ACPOP ss3727548400 Jul 12, 2019 (153)
50 EVA ss3746895392 Jul 12, 2019 (153)
51 PACBIO ss3783586818 Jul 12, 2019 (153)
52 PACBIO ss3789214957 Jul 12, 2019 (153)
53 PACBIO ss3794086965 Jul 12, 2019 (153)
54 KHV_HUMAN_GENOMES ss3799896016 Jul 12, 2019 (153)
55 EVA ss3826461919 Apr 25, 2020 (154)
56 EVA ss3836626190 Apr 25, 2020 (154)
57 EVA ss3842035903 Apr 25, 2020 (154)
58 SGDP_PRJ ss3850153502 Apr 25, 2020 (154)
59 KRGDB ss3895383690 Apr 25, 2020 (154)
60 KOGIC ss3945797978 Apr 25, 2020 (154)
61 TOPMED ss4470801814 Apr 25, 2021 (155)
62 TOMMO_GENOMICS ss5146811278 Apr 25, 2021 (155)
63 1000G_HIGH_COVERAGE ss5244540840 Oct 12, 2022 (156)
64 EVA ss5322500620 Oct 12, 2022 (156)
65 HUGCELL_USP ss5445100585 Oct 12, 2022 (156)
66 1000G_HIGH_COVERAGE ss5517993447 Oct 12, 2022 (156)
67 SANFORD_IMAGENETICS ss5626732063 Oct 12, 2022 (156)
68 TOMMO_GENOMICS ss5674105499 Oct 12, 2022 (156)
69 YY_MCH ss5801323310 Oct 12, 2022 (156)
70 EVA ss5832763877 Oct 12, 2022 (156)
71 EVA ss5849137853 Oct 12, 2022 (156)
72 EVA ss5910526632 Oct 12, 2022 (156)
73 EVA ss5938530133 Oct 12, 2022 (156)
74 EVA ss5979994901 Oct 12, 2022 (156)
75 1000Genomes NC_000001.10 - 164738193 Oct 11, 2018 (152)
76 1000Genomes_30x NC_000001.11 - 164768956 Oct 12, 2022 (156)
77 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 164738193 Oct 11, 2018 (152)
78 Genetic variation in the Estonian population NC_000001.10 - 164738193 Oct 11, 2018 (152)
79 The Danish reference pan genome NC_000001.10 - 164738193 Apr 25, 2020 (154)
80 gnomAD - Genomes NC_000001.11 - 164768956 Apr 25, 2021 (155)
81 Genome of the Netherlands Release 5 NC_000001.10 - 164738193 Apr 25, 2020 (154)
82 KOREAN population from KRGDB NC_000001.10 - 164738193 Apr 25, 2020 (154)
83 Korean Genome Project NC_000001.11 - 164768956 Apr 25, 2020 (154)
84 Northern Sweden NC_000001.10 - 164738193 Jul 12, 2019 (153)
85 Qatari NC_000001.10 - 164738193 Apr 25, 2020 (154)
86 SGDP_PRJ NC_000001.10 - 164738193 Apr 25, 2020 (154)
87 Siberian NC_000001.10 - 164738193 Apr 25, 2020 (154)
88 8.3KJPN NC_000001.10 - 164738193 Apr 25, 2021 (155)
89 14KJPN NC_000001.11 - 164768956 Oct 12, 2022 (156)
90 TopMed NC_000001.11 - 164768956 Apr 25, 2021 (155)
91 UK 10K study - Twins NC_000001.10 - 164738193 Oct 11, 2018 (152)
92 A Vietnamese Genetic Variation Database NC_000001.10 - 164738193 Jul 12, 2019 (153)
93 ALFA NC_000001.11 - 164768956 Apr 25, 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).

Associated ID History Updated (Build)
rs12172726 Mar 11, 2006 (126)
rs60244764 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
2561084, ss3895383690 NC_000001.10:164738192:T:C NC_000001.11:164768955:T:C (self)
ss77512032, ss85561820 NC_000001.8:161469850:T:G NC_000001.11:164768955:T:G (self)
ss87850267, ss111263994, ss164288003, ss167216796, ss199174478, ss205343911, ss210465441, ss253562780, ss276080652, ss290652057, ss1585141688 NC_000001.9:163004816:T:G NC_000001.11:164768955:T:G (self)
4012511, 2186355, 1548151, 1737638, 950719, 2561084, 833265, 1035707, 2170482, 555188, 4780585, 2186355, 469625, ss218688155, ss230759529, ss238402192, ss554789310, ss648463059, ss975757611, ss1068323152, ss1293210974, ss1426000996, ss1574441326, ss1601364730, ss1644358763, ss1795190661, ss1918993777, ss1966884620, ss2020011851, ss2148038834, ss2624514977, ss2698015683, ss2762127656, ss2985528580, ss2987869373, ss3343744009, ss3655809903, ss3727548400, ss3746895392, ss3783586818, ss3789214957, ss3794086965, ss3826461919, ss3836626190, ss3850153502, ss3895383690, ss5146811278, ss5322500620, ss5626732063, ss5832763877, ss5938530133, ss5979994901 NC_000001.10:164738192:T:G NC_000001.11:164768955:T:G (self)
5519382, 29112891, 2175979, 7942603, 34408149, 7183425126, ss2167109492, ss3023763351, ss3646807326, ss3687922706, ss3799896016, ss3842035903, ss3945797978, ss4470801814, ss5244540840, ss5445100585, ss5517993447, ss5674105499, ss5801323310, ss5849137853, ss5910526632 NC_000001.11:164768955:T:G NC_000001.11:164768955:T:G (self)
ss4924195, ss18339051, ss99256772, ss102792339, ss138095139, ss142633214, ss155852840 NT_004487.19:16226834:T:G NC_000001.11:164768955:T:G (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 rs3738196

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