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

rs587780005

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587780005(G;G)
Make rs587780005(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87925541
GenePTEN
is asnp
is mentioned by
dbSNPrs587780005
ebirs587780005
HLIrs587780005
Exacrs587780005
Varsomers587780005
Maprs587780005
PheGenIrs587780005
hapmaprs587780005
1000 genomesrs587780005
hgdprs587780005
ensemblrs587780005
gopubmedrs587780005
geneviewrs587780005
scholarrs587780005
googlers587780005
pharmgkbrs587780005
gwascentralrs587780005
openSNPrs587780005
23andMers587780005
23andMe allrs587780005
SNP Nexus

SNPshotrs587780005
SNPdbers587780005
MSV3drs587780005
GWAS Ctlgrs587780005
Max Magnitude0
ClinVar
Risk rs587780005(G;G)
Alt rs587780005(G;G)
Reference rs587780005(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89685298T>G
CLNSRC
CLNACC RCV000115584.2,