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rs587782603

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782603(G;T)
Make rs587782603(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87952118
GenePTEN
is asnp
is mentioned by
dbSNPrs587782603
ebirs587782603
HLIrs587782603
Exacrs587782603
Varsomers587782603
Maprs587782603
PheGenIrs587782603
hapmaprs587782603
1000 genomesrs587782603
hgdprs587782603
ensemblrs587782603
gopubmedrs587782603
geneviewrs587782603
scholarrs587782603
googlers587782603
pharmgkbrs587782603
gwascentralrs587782603
openSNPrs587782603
23andMers587782603
23andMe allrs587782603
SNP Nexus

SNPshotrs587782603
SNPdbers587782603
MSV3drs587782603
GWAS Ctlgrs587782603
Max Magnitude0
ClinVar
Risk rs587782603(T;T)
Alt rs587782603(T;T)
Reference rs587782603(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.89711875G>T
CLNSRC
CLNACC RCV000131967.2,