Have questions? Visit https://www.reddit.com/r/SNPedia

rs397518443

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397518443(-;-)
Make rs397518443(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1223000
GeneSTK11
is asnp
is mentioned by
dbSNPrs397518443
ebirs397518443
HLIrs397518443
Exacrs397518443
Varsomers397518443
Maprs397518443
PheGenIrs397518443
hapmaprs397518443
1000 genomesrs397518443
hgdprs397518443
ensemblrs397518443
gopubmedrs397518443
geneviewrs397518443
scholarrs397518443
googlers397518443
pharmgkbrs397518443
gwascentralrs397518443
openSNPrs397518443
23andMers397518443
23andMe allrs397518443
SNP Nexus

SNPshotrs397518443
SNPdbers397518443
MSV3drs397518443
GWAS Ctlgrs397518443
Max Magnitude0
ClinVar
Risk rs397518443(;)
Alt rs397518443(;)
Reference rs397518443(A;A)
Significance Pathogenic
Disease Carcinoma of pancreas
Variation info
Gene STK11
CLNDBN Carcinoma of pancreas
Reversed 0
HGVS NC_000019.9:g.1222999delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007880.9,