Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881973

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881973(A;A)
Make rs730881973(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220451
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881973
ebirs730881973
HLIrs730881973
Exacrs730881973
Varsomers730881973
Maprs730881973
PheGenIrs730881973
hapmaprs730881973
1000 genomesrs730881973
hgdprs730881973
ensemblrs730881973
gopubmedrs730881973
geneviewrs730881973
scholarrs730881973
googlers730881973
pharmgkbrs730881973
gwascentralrs730881973
openSNPrs730881973
23andMers730881973
23andMe allrs730881973
SNP Nexus

SNPshotrs730881973
SNPdbers730881973
MSV3drs730881973
GWAS Ctlgrs730881973
Max Magnitude0
ClinVar
Risk rs730881973(A;A)
Alt rs730881973(A;A)
Reference rs730881973(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1220450C>A
CLNSRC
CLNACC RCV000160992.1,