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rs587776658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776658(A;A)
Make rs587776658(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position1220372
GeneSTK11
is asnp
is mentioned by
dbSNPrs587776658
ebirs587776658
HLIrs587776658
Exacrs587776658
Varsomers587776658
Maprs587776658
PheGenIrs587776658
hapmaprs587776658
1000 genomesrs587776658
hgdprs587776658
ensemblrs587776658
gopubmedrs587776658
geneviewrs587776658
scholarrs587776658
googlers587776658
pharmgkbrs587776658
gwascentralrs587776658
openSNPrs587776658
23andMers587776658
23andMe allrs587776658
SNP Nexus

SNPshotrs587776658
SNPdbers587776658
MSV3drs587776658
GWAS Ctlgrs587776658
Max Magnitude0
ClinVar
Risk rs587776658(A;A)
Alt rs587776658(A;A)
Reference rs587776658(G;G)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1220371G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007868.3,