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rs730881974

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881974(C;C)
Make rs730881974(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220453
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881974
ebirs730881974
HLIrs730881974
Exacrs730881974
Varsomers730881974
Maprs730881974
PheGenIrs730881974
hapmaprs730881974
1000 genomesrs730881974
hgdprs730881974
ensemblrs730881974
gopubmedrs730881974
geneviewrs730881974
scholarrs730881974
googlers730881974
pharmgkbrs730881974
gwascentralrs730881974
openSNPrs730881974
23andMers730881974
23andMe allrs730881974
SNP Nexus

SNPshotrs730881974
SNPdbers730881974
MSV3drs730881974
GWAS Ctlgrs730881974
Max Magnitude0
ClinVar
Risk rs730881974(C;C)
Alt rs730881974(C;C)
Reference rs730881974(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.1220452T>C
CLNSRC
CLNACC RCV000160993.1,