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rs587781856

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781856(-;-)
Make rs587781856(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position1220482
GeneSTK11
is asnp
is mentioned by
dbSNPrs587781856
ebirs587781856
HLIrs587781856
Exacrs587781856
Varsomers587781856
Maprs587781856
PheGenIrs587781856
hapmaprs587781856
1000 genomesrs587781856
hgdprs587781856
ensemblrs587781856
gopubmedrs587781856
geneviewrs587781856
scholarrs587781856
googlers587781856
pharmgkbrs587781856
gwascentralrs587781856
openSNPrs587781856
23andMers587781856
23andMe allrs587781856
SNP Nexus

SNPshotrs587781856
SNPdbers587781856
MSV3drs587781856
GWAS Ctlgrs587781856
Max Magnitude0
ClinVar
Risk rs587781856(;)
Alt rs587781856(;)
Reference rs587781856(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1220481delA
CLNSRC
CLNACC RCV000130164.2,