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rs121913323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913323(C;T)
Make rs121913323(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position1220416
GeneSTK11
is asnp
is mentioned by
dbSNPrs121913323
ebirs121913323
HLIrs121913323
Exacrs121913323
Varsomers121913323
Maprs121913323
PheGenIrs121913323
hapmaprs121913323
1000 genomesrs121913323
hgdprs121913323
ensemblrs121913323
gopubmedrs121913323
geneviewrs121913323
scholarrs121913323
googlers121913323
pharmgkbrs121913323
gwascentralrs121913323
openSNPrs121913323
23andMers121913323
23andMe allrs121913323
SNP Nexus

SNPshotrs121913323
SNPdbers121913323
MSV3drs121913323
GWAS Ctlgrs121913323
Max Magnitude0
OMIM602216
Desc
Variant0018
Relatedalso
ClinVar
Risk rs121913323(T;T)
Alt rs121913323(T;T)
Reference rs121913323(C;C)
Significance Pathogenic
Disease Cutaneous malignant melanoma 1
Variation info
Gene STK11
CLNDBN Cutaneous malignant melanoma 1
Reversed 0
HGVS NC_000019.9:g.1220415C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007881.9,