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rs397518442

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397518442(-;-)
Make rs397518442(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220633
GeneSTK11
is asnp
is mentioned by
dbSNPrs397518442
ebirs397518442
HLIrs397518442
Exacrs397518442
Varsomers397518442
Maprs397518442
PheGenIrs397518442
hapmaprs397518442
1000 genomesrs397518442
hgdprs397518442
ensemblrs397518442
gopubmedrs397518442
geneviewrs397518442
scholarrs397518442
googlers397518442
pharmgkbrs397518442
gwascentralrs397518442
openSNPrs397518442
23andMers397518442
23andMe allrs397518442
SNP Nexus

SNPshotrs397518442
SNPdbers397518442
MSV3drs397518442
GWAS Ctlgrs397518442
Max Magnitude0
ClinVar
Risk rs397518442(;)
Alt rs397518442(;)
Reference rs397518442(C;C)
Significance Pathogenic
Disease Carcinoma of pancreas
Variation info
Gene STK11
CLNDBN Carcinoma of pancreas
Reversed 0
HGVS NC_000019.9:g.1220632delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007879.9,