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rs137853079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853079(A;A)
Make rs137853079(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position1207021
GeneSTK11
is asnp
is mentioned by
dbSNPrs137853079
ebirs137853079
HLIrs137853079
Exacrs137853079
Varsomers137853079
Maprs137853079
PheGenIrs137853079
hapmaprs137853079
1000 genomesrs137853079
hgdprs137853079
ensemblrs137853079
gopubmedrs137853079
geneviewrs137853079
scholarrs137853079
googlers137853079
pharmgkbrs137853079
gwascentralrs137853079
openSNPrs137853079
23andMers137853079
23andMe allrs137853079
SNP Nexus

SNPshotrs137853079
SNPdbers137853079
MSV3drs137853079
GWAS Ctlgrs137853079
Max Magnitude0
OMIM602216
Desc
Variant0015
Relatedalso
ClinVar
Risk rs137853079(A,T;A,T)
Alt rs137853079(A,T;A,T)
Reference rs137853079(C;C)
Significance Pathogenic
Disease Carcinoma of pancreas Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene STK11
CLNDBN Carcinoma of pancreas Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000019.9:g.1207020C>A; NC_000019.9:g.1207020C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007878.8, RCV000221907.1,