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rs587782345

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782345(A;G)
Make rs587782345(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87965326
GenePTEN
is asnp
is mentioned by
dbSNPrs587782345
ebirs587782345
HLIrs587782345
Exacrs587782345
Varsomers587782345
Maprs587782345
PheGenIrs587782345
hapmaprs587782345
1000 genomesrs587782345
hgdprs587782345
ensemblrs587782345
gopubmedrs587782345
geneviewrs587782345
scholarrs587782345
googlers587782345
pharmgkbrs587782345
gwascentralrs587782345
openSNPrs587782345
23andMers587782345
23andMe allrs587782345
SNP Nexus

SNPshotrs587782345
SNPdbers587782345
MSV3drs587782345
GWAS Ctlgrs587782345
Max Magnitude0
ClinVar
Risk rs587782345(C,G,T;C,G,T)
Alt rs587782345(C,G,T;C,G,T)
Reference rs587782345(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000010.10:g.89725083A>G; NC_000010.10:g.89725083A>T
CLNSRC
CLNACC RCV000131284.2, RCV000169786.1,