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rs587781254

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781254(G;T)
Make rs587781254(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87933097
GenePTEN
is asnp
is mentioned by
dbSNPrs587781254
ebirs587781254
HLIrs587781254
Exacrs587781254
Varsomers587781254
Maprs587781254
PheGenIrs587781254
hapmaprs587781254
1000 genomesrs587781254
hgdprs587781254
ensemblrs587781254
gopubmedrs587781254
geneviewrs587781254
scholarrs587781254
googlers587781254
pharmgkbrs587781254
gwascentralrs587781254
openSNPrs587781254
23andMers587781254
23andMe allrs587781254
SNP Nexus

SNPshotrs587781254
SNPdbers587781254
MSV3drs587781254
GWAS Ctlgrs587781254
Max Magnitude0
ClinVar
Risk rs587781254(T;T)
Alt rs587781254(T;T)
Reference rs587781254(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692854G>T
CLNSRC
CLNACC RCV000128453.1,