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rs730881983

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881983(G;G)
Make rs730881983(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1221342
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881983
ebirs730881983
HLIrs730881983
Exacrs730881983
Varsomers730881983
Maprs730881983
PheGenIrs730881983
hapmaprs730881983
1000 genomesrs730881983
hgdprs730881983
ensemblrs730881983
gopubmedrs730881983
geneviewrs730881983
scholarrs730881983
googlers730881983
pharmgkbrs730881983
gwascentralrs730881983
openSNPrs730881983
23andMers730881983
23andMe allrs730881983
SNP Nexus

SNPshotrs730881983
SNPdbers730881983
MSV3drs730881983
GWAS Ctlgrs730881983
Max Magnitude0
ClinVar
Risk rs730881983(G;G)
Alt rs730881983(G;G)
Reference rs730881983(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1221341T>G
CLNSRC
CLNACC RCV000161006.1,