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rs137853081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853081(C;C)
Make rs137853081(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position1219352
GeneSTK11
is asnp
is mentioned by
dbSNPrs137853081
ebirs137853081
HLIrs137853081
Exacrs137853081
Varsomers137853081
Maprs137853081
PheGenIrs137853081
hapmaprs137853081
1000 genomesrs137853081
hgdprs137853081
ensemblrs137853081
gopubmedrs137853081
geneviewrs137853081
scholarrs137853081
googlers137853081
pharmgkbrs137853081
gwascentralrs137853081
openSNPrs137853081
23andMers137853081
23andMe allrs137853081
SNP Nexus

SNPshotrs137853081
SNPdbers137853081
MSV3drs137853081
GWAS Ctlgrs137853081
Max Magnitude0
OMIM602216
Desc
Variant0020
Relatedalso
ClinVar
Risk rs137853081(C,T;C,T)
Alt rs137853081(C,T;C,T)
Reference rs137853081(G;G)
Significance Pathogenic
Disease Cutaneous malignant melanoma 1
Variation info
Gene STK11
CLNDBN Cutaneous malignant melanoma 1
Reversed 0
HGVS NC_000019.9:g.1219351G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007883.9,