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rs730881984

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881984(G;T)
Make rs730881984(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1221977
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881984
ebirs730881984
HLIrs730881984
Exacrs730881984
Varsomers730881984
Maprs730881984
PheGenIrs730881984
hapmaprs730881984
1000 genomesrs730881984
hgdprs730881984
ensemblrs730881984
gopubmedrs730881984
geneviewrs730881984
scholarrs730881984
googlers730881984
pharmgkbrs730881984
gwascentralrs730881984
openSNPrs730881984
23andMers730881984
23andMe allrs730881984
SNP Nexus

SNPshotrs730881984
SNPdbers730881984
MSV3drs730881984
GWAS Ctlgrs730881984
Max Magnitude0
ClinVar
Risk rs730881984(T;T)
Alt rs730881984(T;T)
Reference rs730881984(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1221976G>T
CLNSRC
CLNACC RCV000161007.1,