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rs587782455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6.3 Hereditary cancer predisposing syndrome
Make rs587782455(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87960892
GenePTEN
is asnp
is mentioned by
dbSNPrs587782455
dbSNP (old)rs587782455
ClinGenrs587782455
ebirs587782455
HLIrs587782455
Exacrs587782455
Varsomers587782455
Maprs587782455
PheGenIrs587782455
Biobankrs587782455
1000 genomesrs587782455
hgdprs587782455
ensemblrs587782455
gopubmedrs587782455
geneviewrs587782455
scholarrs587782455
googlers587782455
pharmgkbrs587782455
gwascentralrs587782455
openSNPrs587782455
23andMers587782455
23andMe allrs587782455
SNP Nexus

SNPshotrs587782455
SNPdbers587782455
MSV3drs587782455
GWAS Ctlgrs587782455
Max Magnitude6.3
ClinVar
Risk rs587782455(G;G) rs587782455(T;T)
Alt rs587782455(G;G) rs587782455(T;T)
Reference Rs587782455(A;A)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89720649A>G; NC_000010.10:g.89720649A>T
CLNSRC
CLNACC RCV000470021.1, RCV000491383.1, RCV000131528.4, RCV000212884.1,