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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.

rs7438761

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr4:726719 (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
C=0.307590 (81416/264690, TOPMED)
C=0.307873 (43053/139840, GnomAD)
C=0.40566 (11463/28258, 14KJPN) (+ 15 more)
C=0.35657 (6347/17800, ALFA)
C=0.40990 (6870/16760, 8.3KJPN)
C=0.2987 (1913/6404, 1000G_30x)
C=0.3025 (1515/5008, 1000G)
C=0.4670 (2092/4480, Estonian)
C=0.3402 (1311/3854, ALSPAC)
C=0.3409 (1264/3708, TWINSUK)
C=0.3408 (998/2928, KOREAN)
C=0.3521 (645/1832, Korea1K)
C=0.368 (367/998, GoNL)
C=0.365 (219/600, NorthernSweden)
C=0.223 (105/470, SGDP_PRJ)
C=0.102 (22/216, Qatari)
C=0.29 (15/52, Siberian)
C=0.42 (17/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PCGF3 : Intron Variant
LOC124900172 : 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 17800 C=0.35657 G=0.64343, T=0.00000
European Sub 13712 C=0.38433 G=0.61567, T=0.00000
African Sub 2432 C=0.2023 G=0.7977, T=0.0000
African Others Sub 92 C=0.16 G=0.84, T=0.00
African American Sub 2340 C=0.2038 G=0.7962, T=0.0000
Asian Sub 112 C=0.411 G=0.589, T=0.000
East Asian Sub 86 C=0.42 G=0.58, T=0.00
Other Asian Sub 26 C=0.38 G=0.62, T=0.00
Latin American 1 Sub 146 C=0.240 G=0.760, T=0.000
Latin American 2 Sub 610 C=0.462 G=0.538, T=0.000
South Asian Sub 98 C=0.29 G=0.71, T=0.00
Other Sub 690 C=0.281 G=0.719, T=0.000


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=0.307590 G=0.692410
gnomAD - Genomes Global Study-wide 139840 C=0.307873 G=0.692127
gnomAD - Genomes European Sub 75694 C=0.34990 G=0.65010
gnomAD - Genomes African Sub 41922 C=0.19653 G=0.80347
gnomAD - Genomes American Sub 13630 C=0.42069 G=0.57931
gnomAD - Genomes Ashkenazi Jewish Sub 3320 C=0.2265 G=0.7735
gnomAD - Genomes East Asian Sub 3126 C=0.3804 G=0.6196
gnomAD - Genomes Other Sub 2148 C=0.3045 G=0.6955
14KJPN JAPANESE Study-wide 28258 C=0.40566 G=0.59434
Allele Frequency Aggregator Total Global 17800 C=0.35657 G=0.64343, T=0.00000
Allele Frequency Aggregator European Sub 13712 C=0.38433 G=0.61567, T=0.00000
Allele Frequency Aggregator African Sub 2432 C=0.2023 G=0.7977, T=0.0000
Allele Frequency Aggregator Other Sub 690 C=0.281 G=0.719, T=0.000
Allele Frequency Aggregator Latin American 2 Sub 610 C=0.462 G=0.538, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 C=0.240 G=0.760, T=0.000
Allele Frequency Aggregator Asian Sub 112 C=0.411 G=0.589, T=0.000
Allele Frequency Aggregator South Asian Sub 98 C=0.29 G=0.71, T=0.00
8.3KJPN JAPANESE Study-wide 16760 C=0.40990 G=0.59010
1000Genomes_30x Global Study-wide 6404 C=0.2987 G=0.7013
1000Genomes_30x African Sub 1786 C=0.1579 G=0.8421
1000Genomes_30x Europe Sub 1266 C=0.3436 G=0.6564
1000Genomes_30x South Asian Sub 1202 C=0.2729 G=0.7271
1000Genomes_30x East Asian Sub 1170 C=0.3726 G=0.6274
1000Genomes_30x American Sub 980 C=0.441 G=0.559
1000Genomes Global Study-wide 5008 C=0.3025 G=0.6975
1000Genomes African Sub 1322 C=0.1649 G=0.8351
1000Genomes East Asian Sub 1008 C=0.3770 G=0.6230
1000Genomes Europe Sub 1006 C=0.3340 G=0.6660
1000Genomes South Asian Sub 978 C=0.282 G=0.718
1000Genomes American Sub 694 C=0.439 G=0.561
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.4670 G=0.5330
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.3402 G=0.6598
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.3409 G=0.6591
KOREAN population from KRGDB KOREAN Study-wide 2928 C=0.3408 G=0.6592
Korean Genome Project KOREAN Study-wide 1832 C=0.3521 G=0.6479
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.368 G=0.632
Northern Sweden ACPOP Study-wide 600 C=0.365 G=0.635
SGDP_PRJ Global Study-wide 470 C=0.223 G=0.777
Qatari Global Study-wide 216 C=0.102 G=0.898
Siberian Global Study-wide 52 C=0.29 G=0.71
The Danish reference pan genome Danish Study-wide 40 C=0.42 G=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 4 NC_000004.12:g.726719C>G
GRCh38.p14 chr 4 NC_000004.12:g.726719C>T
GRCh37.p13 chr 4 NC_000004.11:g.720508C>G
GRCh37.p13 chr 4 NC_000004.11:g.720508C>T
Gene: PCGF3, polycomb group ring finger 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCGF3 transcript variant 1 NM_001317836.3:c.-288-391…

NM_001317836.3:c.-288-3911C>G

N/A Intron Variant
PCGF3 transcript variant 3 NM_001395245.1:c.-306-391…

NM_001395245.1:c.-306-3911C>G

N/A Intron Variant
PCGF3 transcript variant 4 NM_001395246.1:c.-244-391…

NM_001395246.1:c.-244-3911C>G

N/A Intron Variant
PCGF3 transcript variant 5 NM_001395247.1:c.-289+149…

NM_001395247.1:c.-289+1490C>G

N/A Intron Variant
PCGF3 transcript variant 6 NM_001395248.1:c.-245+149…

NM_001395248.1:c.-245+1490C>G

N/A Intron Variant
PCGF3 transcript variant 7 NM_001395249.1:c.-190+149…

NM_001395249.1:c.-190+1490C>G

N/A Intron Variant
PCGF3 transcript variant 8 NM_001395250.1:c.-432-391…

NM_001395250.1:c.-432-3911C>G

N/A Intron Variant
PCGF3 transcript variant 9 NM_001395251.1:c.-433+149…

NM_001395251.1:c.-433+1490C>G

N/A Intron Variant
PCGF3 transcript variant 2 NM_006315.7:c.-189-3911C>G N/A Intron Variant
PCGF3 transcript variant X1 XM_047449500.1:c. N/A Genic Upstream Transcript Variant
Gene: LOC124900172, uncharacterized LOC124900172 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC124900172 transcript XM_047416540.1:c.*747+264…

XM_047416540.1:c.*747+2644C>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 4 NC_000004.12:g.726719= NC_000004.12:g.726719C>G NC_000004.12:g.726719C>T
GRCh37.p13 chr 4 NC_000004.11:g.720508= NC_000004.11:g.720508C>G NC_000004.11:g.720508C>T
PCGF3 transcript variant 1 NM_001317836.3:c.-288-3911= NM_001317836.3:c.-288-3911C>G NM_001317836.3:c.-288-3911C>T
PCGF3 transcript variant 3 NM_001395245.1:c.-306-3911= NM_001395245.1:c.-306-3911C>G NM_001395245.1:c.-306-3911C>T
PCGF3 transcript variant 4 NM_001395246.1:c.-244-3911= NM_001395246.1:c.-244-3911C>G NM_001395246.1:c.-244-3911C>T
PCGF3 transcript variant 5 NM_001395247.1:c.-289+1490= NM_001395247.1:c.-289+1490C>G NM_001395247.1:c.-289+1490C>T
PCGF3 transcript variant 6 NM_001395248.1:c.-245+1490= NM_001395248.1:c.-245+1490C>G NM_001395248.1:c.-245+1490C>T
PCGF3 transcript variant 7 NM_001395249.1:c.-190+1490= NM_001395249.1:c.-190+1490C>G NM_001395249.1:c.-190+1490C>T
PCGF3 transcript variant 8 NM_001395250.1:c.-432-3911= NM_001395250.1:c.-432-3911C>G NM_001395250.1:c.-432-3911C>T
PCGF3 transcript variant 9 NM_001395251.1:c.-433+1490= NM_001395251.1:c.-433+1490C>G NM_001395251.1:c.-433+1490C>T
PCGF3 transcript NM_006315.4:c.-189-3911= NM_006315.4:c.-189-3911C>G NM_006315.4:c.-189-3911C>T
PCGF3 transcript variant 2 NM_006315.7:c.-189-3911= NM_006315.7:c.-189-3911C>G NM_006315.7:c.-189-3911C>T
PCGF3 transcript variant X1 XM_005272250.1:c.-244-3911= XM_005272250.1:c.-244-3911C>G XM_005272250.1:c.-244-3911C>T
PCGF3 transcript variant X2 XM_005272251.1:c.-189-3911= XM_005272251.1:c.-189-3911C>G XM_005272251.1:c.-189-3911C>T
PCGF3 transcript variant X3 XM_005272252.1:c.-189-3911= XM_005272252.1:c.-189-3911C>G XM_005272252.1:c.-189-3911C>T
PCGF3 transcript variant X3 XM_005272253.1:c.-1437-3911= XM_005272253.1:c.-1437-3911C>G XM_005272253.1:c.-1437-3911C>T
PCGF3 transcript variant X4 XM_005272254.1:c.-1338-3911= XM_005272254.1:c.-1338-3911C>G XM_005272254.1:c.-1338-3911C>T
PCGF3 transcript variant X6 XM_005272255.1:c.-1432-3911= XM_005272255.1:c.-1432-3911C>G XM_005272255.1:c.-1432-3911C>T
PCGF3 transcript variant X7 XM_005272256.1:c.-1338-3911= XM_005272256.1:c.-1338-3911C>G XM_005272256.1:c.-1338-3911C>T
LOC124900172 transcript XM_047416540.1:c.*747+2644= XM_047416540.1:c.*747+2644C>G XM_047416540.1:c.*747+2644C>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#.

77 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss11236212 Jul 11, 2003 (116)
2 WI_SSAHASNP ss14621739 Dec 05, 2003 (119)
3 CSHL-HAPMAP ss17034730 Feb 27, 2004 (120)
4 SSAHASNP ss22133946 Apr 05, 2004 (121)
5 HGSV ss77744999 Dec 07, 2007 (129)
6 HGSV ss84916035 Dec 14, 2007 (130)
7 HGSV ss86050889 Dec 14, 2007 (130)
8 BCMHGSC_JDW ss92436623 Mar 24, 2008 (129)
9 HUMANGENOME_JCVI ss98794619 Feb 03, 2009 (130)
10 BGI ss105798777 Feb 03, 2009 (130)
11 1000GENOMES ss111647112 Jan 25, 2009 (130)
12 1000GENOMES ss112841488 Jan 25, 2009 (130)
13 ILLUMINA-UK ss116834868 Feb 14, 2009 (130)
14 ENSEMBL ss133394182 Dec 01, 2009 (131)
15 ENSEMBL ss139390930 Dec 01, 2009 (131)
16 GMI ss156736908 Dec 01, 2009 (131)
17 COMPLETE_GENOMICS ss162987878 Jul 04, 2010 (132)
18 COMPLETE_GENOMICS ss165986224 Jul 04, 2010 (132)
19 BUSHMAN ss197886258 Jul 04, 2010 (132)
20 BCM-HGSC-SUB ss206557110 Jul 04, 2010 (132)
21 1000GENOMES ss220689546 Jul 14, 2010 (132)
22 1000GENOMES ss232222182 Jul 14, 2010 (132)
23 1000GENOMES ss239551642 Jul 15, 2010 (132)
24 BL ss252869315 May 09, 2011 (134)
25 GMI ss277536389 May 04, 2012 (137)
26 GMI ss284828277 Apr 25, 2013 (138)
27 PJP ss293052568 May 09, 2011 (134)
28 TISHKOFF ss557248905 Apr 25, 2013 (138)
29 SSMP ss651001150 Apr 25, 2013 (138)
30 EVA-GONL ss979664423 Aug 21, 2014 (142)
31 JMKIDD_LAB ss1071210192 Aug 21, 2014 (142)
32 1000GENOMES ss1308054765 Aug 21, 2014 (142)
33 DDI ss1429736945 Apr 01, 2015 (144)
34 EVA_GENOME_DK ss1580377337 Apr 01, 2015 (144)
35 EVA_DECODE ss1589161419 Apr 01, 2015 (144)
36 EVA_UK10K_ALSPAC ss1609220055 Apr 01, 2015 (144)
37 EVA_UK10K_TWINSUK ss1652214088 Apr 01, 2015 (144)
38 HAMMER_LAB ss1800779468 Sep 08, 2015 (146)
39 WEILL_CORNELL_DGM ss1922894389 Feb 12, 2016 (147)
40 GENOMED ss1969636074 Jul 19, 2016 (147)
41 JJLAB ss2022021419 Sep 14, 2016 (149)
42 USC_VALOUEV ss2150126412 Dec 20, 2016 (150)
43 HUMAN_LONGEVITY ss2259754401 Dec 20, 2016 (150)
44 SYSTEMSBIOZJU ss2625511461 Nov 08, 2017 (151)
45 GRF ss2705560896 Nov 08, 2017 (151)
46 GNOMAD ss2804591421 Nov 08, 2017 (151)
47 SWEGEN ss2993978714 Nov 08, 2017 (151)
48 BIOINF_KMB_FNS_UNIBA ss3024780346 Nov 08, 2017 (151)
49 CSHL ss3345494030 Nov 08, 2017 (151)
50 URBANLAB ss3647630988 Oct 12, 2018 (152)
51 EGCUT_WGS ss3661917845 Jul 13, 2019 (153)
52 EVA_DECODE ss3711219099 Jul 13, 2019 (153)
53 ACPOP ss3730770828 Jul 13, 2019 (153)
54 EVA ss3761273637 Jul 13, 2019 (153)
55 PACBIO ss3784592503 Jul 13, 2019 (153)
56 PACBIO ss3790066120 Jul 13, 2019 (153)
57 PACBIO ss3794941142 Jul 13, 2019 (153)
58 KHV_HUMAN_GENOMES ss3804414840 Jul 13, 2019 (153)
59 EVA ss3828322092 Apr 25, 2020 (154)
60 EVA ss3837592159 Apr 25, 2020 (154)
61 EVA ss3843025409 Apr 25, 2020 (154)
62 SGDP_PRJ ss3858003117 Apr 25, 2020 (154)
63 KRGDB ss3904125495 Apr 25, 2020 (154)
64 KOGIC ss3953334188 Apr 25, 2020 (154)
65 TOPMED ss4599904300 Apr 26, 2021 (155)
66 TOMMO_GENOMICS ss5163775494 Apr 26, 2021 (155)
67 1000G_HIGH_COVERAGE ss5257711438 Oct 13, 2022 (156)
68 HUGCELL_USP ss5456671533 Oct 13, 2022 (156)
69 EVA ss5507365652 Oct 13, 2022 (156)
70 1000G_HIGH_COVERAGE ss5537997304 Oct 13, 2022 (156)
71 SANFORD_IMAGENETICS ss5634156990 Oct 13, 2022 (156)
72 TOMMO_GENOMICS ss5697295419 Oct 13, 2022 (156)
73 YY_MCH ss5804669747 Oct 13, 2022 (156)
74 EVA ss5843416319 Oct 13, 2022 (156)
75 EVA ss5854042807 Oct 13, 2022 (156)
76 EVA ss5861782525 Oct 13, 2022 (156)
77 EVA ss5962533138 Oct 13, 2022 (156)
78 1000Genomes NC_000004.11 - 720508 Oct 12, 2018 (152)
79 1000Genomes_30x NC_000004.12 - 726719 Oct 13, 2022 (156)
80 The Avon Longitudinal Study of Parents and Children NC_000004.11 - 720508 Oct 12, 2018 (152)
81 Genetic variation in the Estonian population NC_000004.11 - 720508 Oct 12, 2018 (152)
82 The Danish reference pan genome NC_000004.11 - 720508 Apr 25, 2020 (154)
83 gnomAD - Genomes NC_000004.12 - 726719 Apr 26, 2021 (155)
84 Genome of the Netherlands Release 5 NC_000004.11 - 720508 Apr 25, 2020 (154)
85 KOREAN population from KRGDB NC_000004.11 - 720508 Apr 25, 2020 (154)
86 Korean Genome Project NC_000004.12 - 726719 Apr 25, 2020 (154)
87 Northern Sweden NC_000004.11 - 720508 Jul 13, 2019 (153)
88 Qatari NC_000004.11 - 720508 Apr 25, 2020 (154)
89 SGDP_PRJ NC_000004.11 - 720508 Apr 25, 2020 (154)
90 Siberian NC_000004.11 - 720508 Apr 25, 2020 (154)
91 8.3KJPN NC_000004.11 - 720508 Apr 26, 2021 (155)
92 14KJPN NC_000004.12 - 726719 Oct 13, 2022 (156)
93 TopMed NC_000004.12 - 726719 Apr 26, 2021 (155)
94 UK 10K study - Twins NC_000004.11 - 720508 Oct 12, 2018 (152)
95 ALFA NC_000004.12 - 726719 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).

Associated ID History Updated (Build)
rs56864806 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77744999, ss84916035, ss86050889 NC_000004.9:710507:C:G NC_000004.12:726718:C:G (self)
ss92436623, ss111647112, ss112841488, ss116834868, ss162987878, ss165986224, ss197886258, ss206557110, ss252869315, ss277536389, ss284828277, ss293052568, ss1589161419 NC_000004.10:710507:C:G NC_000004.12:726718:C:G (self)
19391636, 10810696, 7656093, 6542276, 4751921, 11302889, 4055693, 4936319, 10020097, 2642766, 21744801, 10810696, ss220689546, ss232222182, ss239551642, ss557248905, ss651001150, ss979664423, ss1071210192, ss1308054765, ss1429736945, ss1580377337, ss1609220055, ss1652214088, ss1800779468, ss1922894389, ss1969636074, ss2022021419, ss2150126412, ss2625511461, ss2705560896, ss2804591421, ss2993978714, ss3345494030, ss3661917845, ss3730770828, ss3761273637, ss3784592503, ss3790066120, ss3794941142, ss3828322092, ss3837592159, ss3858003117, ss3904125495, ss5163775494, ss5507365652, ss5634156990, ss5843416319, ss5962533138 NC_000004.11:720507:C:G NC_000004.12:726718:C:G (self)
25523239, 137669207, 9712189, 31132523, 437281856, 13012719116, ss2259754401, ss3024780346, ss3647630988, ss3711219099, ss3804414840, ss3843025409, ss3953334188, ss4599904300, ss5257711438, ss5456671533, ss5537997304, ss5697295419, ss5804669747, ss5854042807, ss5861782525 NC_000004.12:726718:C:G NC_000004.12:726718:C:G (self)
ss11236212, ss14621739, ss17034730, ss22133946 NT_037622.3:710507:C:G NC_000004.12:726718:C:G (self)
ss98794619, ss105798777, ss133394182, ss139390930, ss156736908 NT_037622.5:710507:C:G NC_000004.12:726718:C:G (self)
13012719116 NC_000004.12:726718:C:T NC_000004.12:726718: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 rs7438761

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