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rs587776659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587776659(-;-)
Make rs587776659(-;TG)
ReferenceGRCh38 38.1/142
Chromosome19
Position1221312
GeneSTK11
is asnp
is mentioned by
dbSNPrs587776659
ebirs587776659
HLIrs587776659
Exacrs587776659
Varsomers587776659
Maprs587776659
PheGenIrs587776659
hapmaprs587776659
1000 genomesrs587776659
hgdprs587776659
ensemblrs587776659
gopubmedrs587776659
geneviewrs587776659
scholarrs587776659
googlers587776659
pharmgkbrs587776659
gwascentralrs587776659
openSNPrs587776659
23andMers587776659
23andMe allrs587776659
SNP Nexus

SNPshotrs587776659
SNPdbers587776659
MSV3drs587776659
GWAS Ctlgrs587776659
Max Magnitude0
ClinVar
Risk rs587776659(;)
Alt rs587776659(;)
Reference rs587776659(TG;TG)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1221311_1221312delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007870.3,