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

rs730881976

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881976(C;G)
Make rs730881976(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220702
GeneSTK11
is asnp
is mentioned by
dbSNPrs730881976
ebirs730881976
HLIrs730881976
Exacrs730881976
Varsomers730881976
Maprs730881976
PheGenIrs730881976
hapmaprs730881976
1000 genomesrs730881976
hgdprs730881976
ensemblrs730881976
gopubmedrs730881976
geneviewrs730881976
scholarrs730881976
googlers730881976
pharmgkbrs730881976
gwascentralrs730881976
openSNPrs730881976
23andMers730881976
23andMe allrs730881976
SNP Nexus

SNPshotrs730881976
SNPdbers730881976
MSV3drs730881976
GWAS Ctlgrs730881976
Max Magnitude0
ClinVar
Risk rs730881976(G;G)
Alt rs730881976(G;G)
Reference rs730881976(C;C)
Significance Pathogenic
Disease Peutz-Jeghers syndrome Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000019.9:g.1220701C>A; NC_000019.9:g.1220701C>G
CLNSRC
CLNACC RCV000199530.1, RCV000160995.1, RCV000213748.1,