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rs587776660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCCGGCAGC;TCCGGCAGC) 0 common in clinvar
Make rs587776660(-;-)
Make rs587776660(-;TCCGGCAGC)
ReferenceGRCh38 38.1/142
Chromosome19
Position1221994
GeneSTK11
is asnp
is mentioned by
dbSNPrs587776660
ebirs587776660
HLIrs587776660
Exacrs587776660
Varsomers587776660
Maprs587776660
PheGenIrs587776660
hapmaprs587776660
1000 genomesrs587776660
hgdprs587776660
ensemblrs587776660
gopubmedrs587776660
geneviewrs587776660
scholarrs587776660
googlers587776660
pharmgkbrs587776660
gwascentralrs587776660
openSNPrs587776660
23andMers587776660
23andMe allrs587776660
SNP Nexus

SNPshotrs587776660
SNPdbers587776660
MSV3drs587776660
GWAS Ctlgrs587776660
Max Magnitude0
ClinVar
Risk rs587776660(;)
Alt rs587776660(;)
Reference rs587776660(TCCGGCAGC;TCCGGCAGC)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1221993_1222001delTCCGGCAGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007872.4,