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rs587782360

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782360(A;G)
Make rs587782360(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87933162
GenePTEN
is asnp
is mentioned by
dbSNPrs587782360
ebirs587782360
HLIrs587782360
Exacrs587782360
Varsomers587782360
Maprs587782360
PheGenIrs587782360
hapmaprs587782360
1000 genomesrs587782360
hgdprs587782360
ensemblrs587782360
gopubmedrs587782360
geneviewrs587782360
scholarrs587782360
googlers587782360
pharmgkbrs587782360
gwascentralrs587782360
openSNPrs587782360
23andMers587782360
23andMe allrs587782360
SNP Nexus

SNPshotrs587782360
SNPdbers587782360
MSV3drs587782360
GWAS Ctlgrs587782360
Max Magnitude0
ClinVar
Risk rs587782360(G;G)
Alt rs587782360(G;G)
Reference rs587782360(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692919A>G
CLNSRC
CLNACC RCV000131316.2,