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rs121913315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913315(A;A)
Make rs121913315(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position1220488
GeneSTK11
is asnp
is mentioned by
dbSNPrs121913315
ebirs121913315
HLIrs121913315
Exacrs121913315
Varsomers121913315
Maprs121913315
PheGenIrs121913315
hapmaprs121913315
1000 genomesrs121913315
hgdprs121913315
ensemblrs121913315
gopubmedrs121913315
geneviewrs121913315
scholarrs121913315
googlers121913315
pharmgkbrs121913315
gwascentralrs121913315
openSNPrs121913315
23andMers121913315
23andMe allrs121913315
SNP Nexus

SNPshotrs121913315
SNPdbers121913315
MSV3drs121913315
GWAS Ctlgrs121913315
Max Magnitude0
OMIM602216
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121913315(A,T;A,T)
Alt rs121913315(A,T;A,T)
Reference rs121913315(G;G)
Significance Pathogenic
Disease Peutz-Jeghers syndrome Cutaneous malignant melanoma 1
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome Cutaneous malignant melanoma 1
Reversed 0
HGVS NC_000019.9:g.1220487G>A; NC_000019.9:g.1220487G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000168375.1, RCV000007876.8,