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rs730881978

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881978(A;G)
Make rs730881978(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1221975
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881978
ebirs730881978
HLIrs730881978
Exacrs730881978
Varsomers730881978
Maprs730881978
PheGenIrs730881978
hapmaprs730881978
1000 genomesrs730881978
hgdprs730881978
ensemblrs730881978
gopubmedrs730881978
geneviewrs730881978
scholarrs730881978
googlers730881978
pharmgkbrs730881978
gwascentralrs730881978
openSNPrs730881978
23andMers730881978
23andMe allrs730881978
SNP Nexus

SNPshotrs730881978
SNPdbers730881978
MSV3drs730881978
GWAS Ctlgrs730881978
Max Magnitude0
ClinVar
Risk rs730881978(G;G)
Alt rs730881978(G;G)
Reference rs730881978(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1221974A>G
CLNSRC
CLNACC RCV000160997.1,