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rs587782473

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782473(G;G)
Make rs587782473(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87952223
GenePTEN
is asnp
is mentioned by
dbSNPrs587782473
ebirs587782473
HLIrs587782473
Exacrs587782473
Varsomers587782473
Maprs587782473
PheGenIrs587782473
hapmaprs587782473
1000 genomesrs587782473
hgdprs587782473
ensemblrs587782473
gopubmedrs587782473
geneviewrs587782473
scholarrs587782473
googlers587782473
pharmgkbrs587782473
gwascentralrs587782473
openSNPrs587782473
23andMers587782473
23andMe allrs587782473
SNP Nexus

SNPshotrs587782473
SNPdbers587782473
MSV3drs587782473
GWAS Ctlgrs587782473
Max Magnitude0
ClinVar
Risk rs587782473(G;G)
Alt rs587782473(G;G)
Reference rs587782473(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.89711980T>G
CLNSRC
CLNACC RCV000131581.2,