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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.

rs191519212

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr9:131519009 (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=0.000202 (49/243158, GnomAD_exome)
T=0.000891 (125/140240, GnomAD)
T=0.000226 (26/115056, ExAC) (+ 5 more)
T=0.00021 (5/23398, ALFA)
T=0.0008 (5/6404, 1000G_30x)
T=0.0008 (4/5008, 1000G)
T=0.0000 (0/3854, ALSPAC)
T=0.0003 (1/3708, TWINSUK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
POMT1 : Intron Variant
LOC105376301 : 2KB Upstream 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 23398 C=0.99979 G=0.00000, T=0.00021
European Sub 15884 C=1.00000 G=0.00000, T=0.00000
African Sub 3532 C=0.9989 G=0.0000, T=0.0011
African Others Sub 122 C=1.000 G=0.000, T=0.000
African American Sub 3410 C=0.9988 G=0.0000, T=0.0012
Asian Sub 168 C=1.000 G=0.000, T=0.000
East Asian Sub 112 C=1.000 G=0.000, T=0.000
Other Asian Sub 56 C=1.00 G=0.00, T=0.00
Latin American 1 Sub 146 C=1.000 G=0.000, T=0.000
Latin American 2 Sub 610 C=1.000 G=0.000, T=0.000
South Asian Sub 98 C=1.00 G=0.00, T=0.00
Other Sub 2960 C=0.9997 G=0.0000, T=0.0003


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
gnomAD - Exomes Global Study-wide 243158 C=0.999798 T=0.000202
gnomAD - Exomes European Sub 129068 C=0.999930 T=0.000070
gnomAD - Exomes Asian Sub 48664 C=1.00000 T=0.00000
gnomAD - Exomes American Sub 34370 C=0.99991 T=0.00009
gnomAD - Exomes African Sub 15156 C=0.99762 T=0.00238
gnomAD - Exomes Ashkenazi Jewish Sub 9898 C=1.0000 T=0.0000
gnomAD - Exomes Other Sub 6002 C=0.9998 T=0.0002
gnomAD - Genomes Global Study-wide 140240 C=0.999109 T=0.000891
gnomAD - Genomes European Sub 75948 C=0.99997 T=0.00003
gnomAD - Genomes African Sub 42032 C=0.99755 T=0.00245
gnomAD - Genomes American Sub 13652 C=0.99883 T=0.00117
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=1.0000 T=0.0000
gnomAD - Genomes East Asian Sub 3130 C=1.0000 T=0.0000
gnomAD - Genomes Other Sub 2154 C=0.9981 T=0.0019
ExAC Global Study-wide 115056 C=0.999774 T=0.000226
ExAC Europe Sub 68904 C=0.99996 T=0.00004
ExAC Asian Sub 24768 C=1.00000 T=0.00000
ExAC American Sub 11324 C=0.99991 T=0.00009
ExAC African Sub 9208 C=0.9977 T=0.0023
ExAC Other Sub 852 C=0.999 T=0.001
Allele Frequency Aggregator Total Global 23398 C=0.99979 G=0.00000, T=0.00021
Allele Frequency Aggregator European Sub 15884 C=1.00000 G=0.00000, T=0.00000
Allele Frequency Aggregator African Sub 3532 C=0.9989 G=0.0000, T=0.0011
Allele Frequency Aggregator Other Sub 2960 C=0.9997 G=0.0000, T=0.0003
Allele Frequency Aggregator Latin American 2 Sub 610 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator Asian Sub 168 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 C=1.000 G=0.000, T=0.000
Allele Frequency Aggregator South Asian Sub 98 C=1.00 G=0.00, T=0.00
1000Genomes_30x Global Study-wide 6404 C=0.9992 T=0.0008
1000Genomes_30x African Sub 1786 C=0.9983 T=0.0017
1000Genomes_30x Europe Sub 1266 C=1.0000 T=0.0000
1000Genomes_30x South Asian Sub 1202 C=1.0000 T=0.0000
1000Genomes_30x East Asian Sub 1170 C=1.0000 T=0.0000
1000Genomes_30x American Sub 980 C=0.998 T=0.002
1000Genomes Global Study-wide 5008 C=0.9992 T=0.0008
1000Genomes African Sub 1322 C=0.9977 T=0.0023
1000Genomes East Asian Sub 1008 C=1.0000 T=0.0000
1000Genomes Europe Sub 1006 C=1.0000 T=0.0000
1000Genomes South Asian Sub 978 C=1.000 T=0.000
1000Genomes American Sub 694 C=0.999 T=0.001
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=1.0000 T=0.0000
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.9997 T=0.0003
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 9 NC_000009.12:g.131519009C>G
GRCh38.p14 chr 9 NC_000009.12:g.131519009C>T
GRCh37.p13 chr 9 NC_000009.11:g.134394396C>G
GRCh37.p13 chr 9 NC_000009.11:g.134394396C>T
POMT1 RefSeqGene (LRG_842) NG_008896.2:g.21108C>G
POMT1 RefSeqGene (LRG_842) NG_008896.2:g.21108C>T
Gene: POMT1, protein O-mannosyltransferase 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
POMT1 transcript variant 2 NM_001077365.2:c.1486+52C…

NM_001077365.2:c.1486+52C>G

N/A Intron Variant
POMT1 transcript variant 3 NM_001077366.2:c.1324+52C…

NM_001077366.2:c.1324+52C>G

N/A Intron Variant
POMT1 transcript variant 4 NM_001136113.2:c.1486+52C…

NM_001136113.2:c.1486+52C>G

N/A Intron Variant
POMT1 transcript variant 5 NM_001136114.2:c.1135+52C…

NM_001136114.2:c.1135+52C>G

N/A Intron Variant
POMT1 transcript variant 6 NM_001353193.2:c.1552+52C…

NM_001353193.2:c.1552+52C>G

N/A Intron Variant
POMT1 transcript variant 7 NM_001353194.2:c.1324+52C…

NM_001353194.2:c.1324+52C>G

N/A Intron Variant
POMT1 transcript variant 8 NM_001353195.2:c.1135+52C…

NM_001353195.2:c.1135+52C>G

N/A Intron Variant
POMT1 transcript variant 9 NM_001353196.2:c.1396+52C…

NM_001353196.2:c.1396+52C>G

N/A Intron Variant
POMT1 transcript variant 10 NM_001353197.2:c.1390+52C…

NM_001353197.2:c.1390+52C>G

N/A Intron Variant
POMT1 transcript variant 11 NM_001353198.2:c.1390+52C…

NM_001353198.2:c.1390+52C>G

N/A Intron Variant
POMT1 transcript variant 12 NM_001353199.2:c.1201+52C…

NM_001353199.2:c.1201+52C>G

N/A Intron Variant
POMT1 transcript variant 13 NM_001353200.2:c.1030+52C…

NM_001353200.2:c.1030+52C>G

N/A Intron Variant
POMT1 transcript variant 24 NM_001374689.1:c.1474+52C…

NM_001374689.1:c.1474+52C>G

N/A Intron Variant
POMT1 transcript variant 25 NM_001374690.1:c.1365+472…

NM_001374690.1:c.1365+472C>G

N/A Intron Variant
POMT1 transcript variant 26 NM_001374691.1:c.1135+52C…

NM_001374691.1:c.1135+52C>G

N/A Intron Variant
POMT1 transcript variant 27 NM_001374692.1:c.1135+52C…

NM_001374692.1:c.1135+52C>G

N/A Intron Variant
POMT1 transcript variant 28 NM_001374693.1:c.1135+52C…

NM_001374693.1:c.1135+52C>G

N/A Intron Variant
POMT1 transcript variant 29 NM_001374695.1:c.1096+52C…

NM_001374695.1:c.1096+52C>G

N/A Intron Variant
POMT1 transcript variant 1 NM_007171.4:c.1552+52C>G N/A Intron Variant
POMT1 transcript variant 14 NR_148391.2:n. N/A Intron Variant
POMT1 transcript variant 15 NR_148392.2:n. N/A Intron Variant
POMT1 transcript variant 16 NR_148393.2:n. N/A Intron Variant
POMT1 transcript variant 17 NR_148394.2:n. N/A Intron Variant
POMT1 transcript variant 18 NR_148395.2:n. N/A Intron Variant
POMT1 transcript variant 19 NR_148396.2:n. N/A Intron Variant
POMT1 transcript variant 20 NR_148397.2:n. N/A Intron Variant
POMT1 transcript variant 21 NR_148398.2:n. N/A Intron Variant
POMT1 transcript variant 22 NR_148399.2:n. N/A Intron Variant
POMT1 transcript variant 23 NR_148400.2:n. N/A Intron Variant
POMT1 transcript variant X2 XM_011518140.3:c.1405+52C…

XM_011518140.3:c.1405+52C>G

N/A Intron Variant
POMT1 transcript variant X3 XM_011518141.3:c.1339+52C…

XM_011518141.3:c.1339+52C>G

N/A Intron Variant
POMT1 transcript variant X6 XM_011518142.3:c.1243+52C…

XM_011518142.3:c.1243+52C>G

N/A Intron Variant
POMT1 transcript variant X7 XM_011518143.3:c.1237+52C…

XM_011518143.3:c.1237+52C>G

N/A Intron Variant
POMT1 transcript variant X12 XM_011518145.3:c.1096+52C…

XM_011518145.3:c.1096+52C>G

N/A Intron Variant
POMT1 transcript variant X14 XM_024447380.2:c.355+52C>G N/A Intron Variant
POMT1 transcript variant X8 XM_047422640.1:c.1177+52C…

XM_047422640.1:c.1177+52C>G

N/A Intron Variant
POMT1 transcript variant X14 XM_047422642.1:c.424+52C>G N/A Intron Variant
POMT1 transcript variant X10 XM_047422641.1:c. N/A Genic Downstream Transcript Variant
POMT1 transcript variant X1 XR_001746160.3:n. N/A Intron Variant
POMT1 transcript variant X4 XR_007061226.1:n. N/A Intron Variant
POMT1 transcript variant X5 XR_007061227.1:n. N/A Intron Variant
POMT1 transcript variant X9 XR_007061228.1:n. N/A Intron Variant
POMT1 transcript variant X11 XR_007061229.1:n. N/A Intron Variant
POMT1 transcript variant X13 XR_007061230.1:n. N/A Intron Variant
Gene: LOC105376301, uncharacterized LOC105376301 (minus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
LOC105376301 transcript XR_930402.3:n. N/A Upstream 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 C= G T
GRCh38.p14 chr 9 NC_000009.12:g.131519009= NC_000009.12:g.131519009C>G NC_000009.12:g.131519009C>T
GRCh37.p13 chr 9 NC_000009.11:g.134394396= NC_000009.11:g.134394396C>G NC_000009.11:g.134394396C>T
POMT1 RefSeqGene (LRG_842) NG_008896.2:g.21108= NG_008896.2:g.21108C>G NG_008896.2:g.21108C>T
POMT1 transcript variant 2 NM_001077365.1:c.1486+52= NM_001077365.1:c.1486+52C>G NM_001077365.1:c.1486+52C>T
POMT1 transcript variant 2 NM_001077365.2:c.1486+52= NM_001077365.2:c.1486+52C>G NM_001077365.2:c.1486+52C>T
POMT1 transcript variant 3 NM_001077366.1:c.1324+52= NM_001077366.1:c.1324+52C>G NM_001077366.1:c.1324+52C>T
POMT1 transcript variant 3 NM_001077366.2:c.1324+52= NM_001077366.2:c.1324+52C>G NM_001077366.2:c.1324+52C>T
POMT1 transcript variant 4 NM_001136113.1:c.1486+52= NM_001136113.1:c.1486+52C>G NM_001136113.1:c.1486+52C>T
POMT1 transcript variant 4 NM_001136113.2:c.1486+52= NM_001136113.2:c.1486+52C>G NM_001136113.2:c.1486+52C>T
POMT1 transcript variant 5 NM_001136114.1:c.1135+52= NM_001136114.1:c.1135+52C>G NM_001136114.1:c.1135+52C>T
POMT1 transcript variant 5 NM_001136114.2:c.1135+52= NM_001136114.2:c.1135+52C>G NM_001136114.2:c.1135+52C>T
POMT1 transcript variant 6 NM_001353193.2:c.1552+52= NM_001353193.2:c.1552+52C>G NM_001353193.2:c.1552+52C>T
POMT1 transcript variant 7 NM_001353194.2:c.1324+52= NM_001353194.2:c.1324+52C>G NM_001353194.2:c.1324+52C>T
POMT1 transcript variant 8 NM_001353195.2:c.1135+52= NM_001353195.2:c.1135+52C>G NM_001353195.2:c.1135+52C>T
POMT1 transcript variant 9 NM_001353196.2:c.1396+52= NM_001353196.2:c.1396+52C>G NM_001353196.2:c.1396+52C>T
POMT1 transcript variant 10 NM_001353197.2:c.1390+52= NM_001353197.2:c.1390+52C>G NM_001353197.2:c.1390+52C>T
POMT1 transcript variant 11 NM_001353198.2:c.1390+52= NM_001353198.2:c.1390+52C>G NM_001353198.2:c.1390+52C>T
POMT1 transcript variant 12 NM_001353199.2:c.1201+52= NM_001353199.2:c.1201+52C>G NM_001353199.2:c.1201+52C>T
POMT1 transcript variant 13 NM_001353200.2:c.1030+52= NM_001353200.2:c.1030+52C>G NM_001353200.2:c.1030+52C>T
POMT1 transcript variant 24 NM_001374689.1:c.1474+52= NM_001374689.1:c.1474+52C>G NM_001374689.1:c.1474+52C>T
POMT1 transcript variant 25 NM_001374690.1:c.1365+472= NM_001374690.1:c.1365+472C>G NM_001374690.1:c.1365+472C>T
POMT1 transcript variant 26 NM_001374691.1:c.1135+52= NM_001374691.1:c.1135+52C>G NM_001374691.1:c.1135+52C>T
POMT1 transcript variant 27 NM_001374692.1:c.1135+52= NM_001374692.1:c.1135+52C>G NM_001374692.1:c.1135+52C>T
POMT1 transcript variant 28 NM_001374693.1:c.1135+52= NM_001374693.1:c.1135+52C>G NM_001374693.1:c.1135+52C>T
POMT1 transcript variant 29 NM_001374695.1:c.1096+52= NM_001374695.1:c.1096+52C>G NM_001374695.1:c.1096+52C>T
POMT1 transcript variant 1 NM_007171.3:c.1552+52= NM_007171.3:c.1552+52C>G NM_007171.3:c.1552+52C>T
POMT1 transcript variant 1 NM_007171.4:c.1552+52= NM_007171.4:c.1552+52C>G NM_007171.4:c.1552+52C>T
POMT1 transcript variant X6 XM_005272156.1:c.1552+52= XM_005272156.1:c.1552+52C>G XM_005272156.1:c.1552+52C>T
POMT1 transcript variant X2 XM_005272157.1:c.1396+52= XM_005272157.1:c.1396+52C>G XM_005272157.1:c.1396+52C>T
POMT1 transcript variant X7 XM_005272158.1:c.1390+52= XM_005272158.1:c.1390+52C>G XM_005272158.1:c.1390+52C>T
POMT1 transcript variant X11 XM_005272159.1:c.1201+52= XM_005272159.1:c.1201+52C>G XM_005272159.1:c.1201+52C>T
POMT1 transcript variant X5 XM_005272160.1:c.820+52= XM_005272160.1:c.820+52C>G XM_005272160.1:c.820+52C>T
POMT1 transcript variant X6 XM_005272161.1:c.355+52= XM_005272161.1:c.355+52C>G XM_005272161.1:c.355+52C>T
POMT1 transcript variant X14 XM_005272162.1:c.355+52= XM_005272162.1:c.355+52C>G XM_005272162.1:c.355+52C>T
POMT1 transcript variant X2 XM_011518140.3:c.1405+52= XM_011518140.3:c.1405+52C>G XM_011518140.3:c.1405+52C>T
POMT1 transcript variant X3 XM_011518141.3:c.1339+52= XM_011518141.3:c.1339+52C>G XM_011518141.3:c.1339+52C>T
POMT1 transcript variant X6 XM_011518142.3:c.1243+52= XM_011518142.3:c.1243+52C>G XM_011518142.3:c.1243+52C>T
POMT1 transcript variant X7 XM_011518143.3:c.1237+52= XM_011518143.3:c.1237+52C>G XM_011518143.3:c.1237+52C>T
POMT1 transcript variant X12 XM_011518145.3:c.1096+52= XM_011518145.3:c.1096+52C>G XM_011518145.3:c.1096+52C>T
POMT1 transcript variant X14 XM_024447380.2:c.355+52= XM_024447380.2:c.355+52C>G XM_024447380.2:c.355+52C>T
POMT1 transcript variant X8 XM_047422640.1:c.1177+52= XM_047422640.1:c.1177+52C>G XM_047422640.1:c.1177+52C>T
POMT1 transcript variant X14 XM_047422642.1:c.424+52= XM_047422642.1:c.424+52C>G XM_047422642.1:c.424+52C>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#.

18 SubSNP, 10 Frequency submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss461349391 Sep 17, 2011 (135)
2 1000GENOMES ss1335683858 Aug 21, 2014 (142)
3 EVA_UK10K_ALSPAC ss1623685249 Apr 01, 2015 (144)
4 EVA_UK10K_TWINSUK ss1666679282 Apr 01, 2015 (144)
5 EVA_EXAC ss1689707955 Apr 01, 2015 (144)
6 HUMAN_LONGEVITY ss2314913465 Dec 20, 2016 (150)
7 GNOMAD ss2737949995 Nov 08, 2017 (151)
8 GNOMAD ss2748292181 Nov 08, 2017 (151)
9 GNOMAD ss2883870826 Nov 08, 2017 (151)
10 TOPMED ss4837656239 Apr 26, 2021 (155)
11 TOPMED ss4837656240 Apr 26, 2021 (155)
12 1000G_HIGH_COVERAGE ss5282382958 Oct 16, 2022 (156)
13 EVA ss5390631172 Oct 16, 2022 (156)
14 HUGCELL_USP ss5478230370 Oct 16, 2022 (156)
15 1000G_HIGH_COVERAGE ss5575539166 Oct 16, 2022 (156)
16 SANFORD_IMAGENETICS ss5648375943 Oct 16, 2022 (156)
17 EVA ss5918258063 Oct 16, 2022 (156)
18 EVA ss5977589848 Oct 16, 2022 (156)
19 1000Genomes NC_000009.11 - 134394396 Oct 12, 2018 (152)
20 1000Genomes_30x NC_000009.12 - 131519009 Oct 16, 2022 (156)
21 The Avon Longitudinal Study of Parents and Children NC_000009.11 - 134394396 Oct 12, 2018 (152)
22 ExAC NC_000009.11 - 134394396 Oct 12, 2018 (152)
23 gnomAD - Genomes NC_000009.12 - 131519009 Apr 26, 2021 (155)
24 gnomAD - Exomes NC_000009.11 - 134394396 Jul 13, 2019 (153)
25 TopMed

Submission ignored due to conflicting rows:
Row 675033800 (NC_000009.12:131519008:C:G 1/264690)
Row 675033801 (NC_000009.12:131519008:C:T 239/264690)

- Apr 26, 2021 (155)
26 TopMed

Submission ignored due to conflicting rows:
Row 675033800 (NC_000009.12:131519008:C:G 1/264690)
Row 675033801 (NC_000009.12:131519008:C:T 239/264690)

- Apr 26, 2021 (155)
27 UK 10K study - Twins NC_000009.11 - 134394396 Oct 12, 2018 (152)
28 ALFA NC_000009.12 - 131519009 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
2938479138, ss4837656239 NC_000009.12:131519008:C:G NC_000009.12:131519008:C:G (self)
48010256, 26683793, 9847438, 7139257, 26683793, ss461349391, ss1335683858, ss1623685249, ss1666679282, ss1689707955, ss2737949995, ss2748292181, ss2883870826, ss5390631172, ss5648375943, ss5977589848 NC_000009.11:134394395:C:T NC_000009.12:131519008:C:T (self)
63065101, 339329229, 2938479138, ss2314913465, ss4837656240, ss5282382958, ss5478230370, ss5575539166, ss5918258063 NC_000009.12:131519008:C:T NC_000009.12:131519008: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 rs191519212

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