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rs121913325

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913325(A;A)
Make rs121913325(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1223060
GeneSTK11
is asnp
is mentioned by
dbSNPrs121913325
dbSNP (old)rs121913325
ClinGenrs121913325
ebirs121913325
HLIrs121913325
Exacrs121913325
Gnomadrs121913325
Varsomers121913325
LitVarrs121913325
Maprs121913325
PheGenIrs121913325
Biobankrs121913325
1000 genomesrs121913325
hgdprs121913325
ensemblrs121913325
gopubmedrs121913325
geneviewrs121913325
scholarrs121913325
googlers121913325
pharmgkbrs121913325
gwascentralrs121913325
openSNPrs121913325
23andMers121913325
23andMe allrs121913325
SNPshotrs121913325
SNPdbers121913325
MSV3drs121913325
GWAS Ctlgrs121913325
Max Magnitude0
ClinVar
Risk rs121913325(A;A)
Alt rs121913325(A;A)
Reference Rs121913325(G;G)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene STK11
CLNDBN Neoplasm
Reversed 0
HGVS NC_000019.9:g.1223059G>A
CLNSRC
CLNACC RCV000425766.1,