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rs137853080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853080(G;G)
Make rs137853080(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position1207058
GeneSTK11
is asnp
is mentioned by
dbSNPrs137853080
ebirs137853080
HLIrs137853080
Exacrs137853080
Varsomers137853080
Maprs137853080
PheGenIrs137853080
hapmaprs137853080
1000 genomesrs137853080
hgdprs137853080
ensemblrs137853080
gopubmedrs137853080
geneviewrs137853080
scholarrs137853080
googlers137853080
pharmgkbrs137853080
gwascentralrs137853080
openSNPrs137853080
23andMers137853080
23andMe allrs137853080
SNP Nexus

SNPshotrs137853080
SNPdbers137853080
MSV3drs137853080
GWAS Ctlgrs137853080
Max Magnitude0
OMIM602216
Desc
Variant0019
Relatedalso
ClinVar
Risk rs137853080(G;G)
Alt rs137853080(G;G)
Reference rs137853080(T;T)
Significance Pathogenic
Disease Cutaneous malignant melanoma 1
Variation info
Gene STK11
CLNDBN Cutaneous malignant melanoma 1
Reversed 0
HGVS NC_000019.9:g.1207057T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007882.9,