Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781912

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs587781912(-;-)
Make rs587781912(-;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87864519
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs587781912
ebirs587781912
HLIrs587781912
Exacrs587781912
Varsomers587781912
Maprs587781912
PheGenIrs587781912
hapmaprs587781912
1000 genomesrs587781912
hgdprs587781912
ensemblrs587781912
gopubmedrs587781912
geneviewrs587781912
scholarrs587781912
googlers587781912
pharmgkbrs587781912
gwascentralrs587781912
openSNPrs587781912
23andMers587781912
23andMe allrs587781912
SNP Nexus

SNPshotrs587781912
SNPdbers587781912
MSV3drs587781912
GWAS Ctlgrs587781912
Max Magnitude0
ClinVar
Risk rs587781912(;)
Alt rs587781912(;)
Reference rs587781912(AA;AA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89624276_89624277delAA
CLNSRC
CLNACC RCV000130255.2,