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rs730881972

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881972(C;C)
Make rs730881972(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220395
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881972
ebirs730881972
HLIrs730881972
Exacrs730881972
Varsomers730881972
Maprs730881972
PheGenIrs730881972
hapmaprs730881972
1000 genomesrs730881972
hgdprs730881972
ensemblrs730881972
gopubmedrs730881972
geneviewrs730881972
scholarrs730881972
googlers730881972
pharmgkbrs730881972
gwascentralrs730881972
openSNPrs730881972
23andMers730881972
23andMe allrs730881972
SNP Nexus

SNPshotrs730881972
SNPdbers730881972
MSV3drs730881972
GWAS Ctlgrs730881972
Max Magnitude0
ClinVar
Risk rs730881972(C;C)
Alt rs730881972(C;C)
Reference rs730881972(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.1220394G>C
CLNSRC
CLNACC RCV000160991.1,