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rs121913316

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913316(A;T)
Make rs121913316(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1220489
GeneSTK11
is asnp
is mentioned by
dbSNPrs121913316
dbSNP (old)rs121913316
ClinGenrs121913316
ebirs121913316
HLIrs121913316
Exacrs121913316
Gnomadrs121913316
Varsomers121913316
Maprs121913316
PheGenIrs121913316
Biobankrs121913316
1000 genomesrs121913316
hgdprs121913316
ensemblrs121913316
gopubmedrs121913316
geneviewrs121913316
scholarrs121913316
googlers121913316
pharmgkbrs121913316
gwascentralrs121913316
openSNPrs121913316
23andMers121913316
23andMe allrs121913316
SNPshotrs121913316
SNPdbers121913316
MSV3drs121913316
GWAS Ctlgrs121913316
Max Magnitude0
ClinVar
Risk rs121913316(T;T)
Alt rs121913316(T;T)
Reference Rs121913316(A;A)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene STK11
CLNDBN Neoplasm
Reversed 0
HGVS NC_000019.9:g.1220488A>T
CLNSRC
CLNACC RCV000437343.1,