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rs730881977

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881977(A;A)
Make rs730881977(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1221230
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881977
ebirs730881977
HLIrs730881977
Exacrs730881977
Varsomers730881977
Maprs730881977
PheGenIrs730881977
hapmaprs730881977
1000 genomesrs730881977
hgdprs730881977
ensemblrs730881977
gopubmedrs730881977
geneviewrs730881977
scholarrs730881977
googlers730881977
pharmgkbrs730881977
gwascentralrs730881977
openSNPrs730881977
23andMers730881977
23andMe allrs730881977
SNP Nexus

SNPshotrs730881977
SNPdbers730881977
MSV3drs730881977
GWAS Ctlgrs730881977
Max Magnitude0
ClinVar
Risk rs730881977(A;A)
Alt rs730881977(A;A)
Reference rs730881977(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1221229G>A
CLNSRC
CLNACC RCV000160996.1,