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rs587782316

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782316(A;A)
Make rs587782316(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87952145
GenePTEN
is asnp
is mentioned by
dbSNPrs587782316
ebirs587782316
HLIrs587782316
Exacrs587782316
Varsomers587782316
Maprs587782316
PheGenIrs587782316
hapmaprs587782316
1000 genomesrs587782316
hgdprs587782316
ensemblrs587782316
gopubmedrs587782316
geneviewrs587782316
scholarrs587782316
googlers587782316
pharmgkbrs587782316
gwascentralrs587782316
openSNPrs587782316
23andMers587782316
23andMe allrs587782316
SNP Nexus

SNPshotrs587782316
SNPdbers587782316
MSV3drs587782316
GWAS Ctlgrs587782316
Max Magnitude0
ClinVar
Risk rs587782316(A;A)
Alt rs587782316(A;A)
Reference rs587782316(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.89711902T>A
CLNSRC
CLNACC RCV000131215.2,