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rs587776657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGTC;GGTC) 0 common in clinvar
Make rs587776657(-;-)
Make rs587776657(-;TCGG)
Make rs587776657(TCGG;TCGG)
ReferenceGRCh38 38.1/142
Chromosome19
Position1220701
GeneSTK11
is asnp
is mentioned by
dbSNPrs587776657
ebirs587776657
HLIrs587776657
Exacrs587776657
Varsomers587776657
Maprs587776657
PheGenIrs587776657
hapmaprs587776657
1000 genomesrs587776657
hgdprs587776657
ensemblrs587776657
gopubmedrs587776657
geneviewrs587776657
scholarrs587776657
googlers587776657
pharmgkbrs587776657
gwascentralrs587776657
openSNPrs587776657
23andMers587776657
23andMe allrs587776657
SNP Nexus

SNPshotrs587776657
SNPdbers587776657
MSV3drs587776657
GWAS Ctlgrs587776657
Max Magnitude0
ClinVar
Risk rs587776657(;)
Alt rs587776657(;)
Reference rs587776657(GGTC;GGTC)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1220700_1220703delTCGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007867.3,