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rs876658584

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658584(A;G)
Make rs876658584(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position1218415
GeneSTK11
is asnp
is mentioned by
dbSNPrs876658584
ebirs876658584
HLIrs876658584
Exacrs876658584
Varsomers876658584
Maprs876658584
PheGenIrs876658584
hapmaprs876658584
1000 genomesrs876658584
hgdprs876658584
ensemblrs876658584
gopubmedrs876658584
geneviewrs876658584
scholarrs876658584
googlers876658584
pharmgkbrs876658584
gwascentralrs876658584
openSNPrs876658584
23andMers876658584
23andMe allrs876658584
SNP Nexus

SNPshotrs876658584
SNPdbers876658584
MSV3drs876658584
GWAS Ctlgrs876658584
Max Magnitude0
ClinVar
Risk rs876658584(G;G)
Alt rs876658584(G;G)
Reference rs876658584(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene STK11
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000019.9:g.1218414A>G
CLNSRC
CLNACC RCV000222975.1,