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rs587776661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776661(-;-)
Make rs587776661(-;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position1221977
GeneSTK11
is asnp
is mentioned by
dbSNPrs587776661
ebirs587776661
HLIrs587776661
Exacrs587776661
Varsomers587776661
Maprs587776661
PheGenIrs587776661
hapmaprs587776661
1000 genomesrs587776661
hgdprs587776661
ensemblrs587776661
gopubmedrs587776661
geneviewrs587776661
scholarrs587776661
googlers587776661
pharmgkbrs587776661
gwascentralrs587776661
openSNPrs587776661
23andMers587776661
23andMe allrs587776661
SNP Nexus

SNPshotrs587776661
SNPdbers587776661
MSV3drs587776661
GWAS Ctlgrs587776661
Max Magnitude0
ClinVar
Risk rs587776661(;)
Alt rs587776661(;)
Reference rs587776661(G;G)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1221976delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007885.4,