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

rs587776667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776667(A;A)
Make rs587776667(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position87931090
GenePTEN
is asnp
is mentioned by
dbSNPrs587776667
ebirs587776667
HLIrs587776667
Exacrs587776667
Varsomers587776667
Maprs587776667
PheGenIrs587776667
hapmaprs587776667
1000 genomesrs587776667
hgdprs587776667
ensemblrs587776667
gopubmedrs587776667
geneviewrs587776667
scholarrs587776667
googlers587776667
pharmgkbrs587776667
gwascentralrs587776667
openSNPrs587776667
23andMers587776667
23andMe allrs587776667
SNP Nexus

SNPshotrs587776667
SNPdbers587776667
MSV3drs587776667
GWAS Ctlgrs587776667
Max Magnitude0
ClinVar
Risk rs587776667(A,T;A,T)
Alt rs587776667(A,T;A,T)
Reference rs587776667(G;G)
Significance Pathogenic
Disease Endometrial carcinoma not provided
Variation info
Gene PTEN
CLNDBN Endometrial carcinoma not provided
Reversed 0
HGVS NC_000010.10:g.89690847G>A; NC_000010.10:g.89690847G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008266.3, RCV000169865.2,