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

rs587782607

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782607(A;A)
Make rs587782607(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87960914
GenePTEN
is asnp
is mentioned by
dbSNPrs587782607
ebirs587782607
HLIrs587782607
Exacrs587782607
Varsomers587782607
Maprs587782607
PheGenIrs587782607
hapmaprs587782607
1000 genomesrs587782607
hgdprs587782607
ensemblrs587782607
gopubmedrs587782607
geneviewrs587782607
scholarrs587782607
googlers587782607
pharmgkbrs587782607
gwascentralrs587782607
openSNPrs587782607
23andMers587782607
23andMe allrs587782607
SNP Nexus

SNPshotrs587782607
SNPdbers587782607
MSV3drs587782607
GWAS Ctlgrs587782607
Max Magnitude0
ClinVar
Risk rs587782607(A;A)
Alt rs587782607(A;A)
Reference rs587782607(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89720671G>A
CLNSRC
CLNACC RCV000131976.2,