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rs587782350

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782350(C;T)
Make rs587782350(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87957955
GenePTEN
is asnp
is mentioned by
dbSNPrs587782350
ebirs587782350
HLIrs587782350
Exacrs587782350
Varsomers587782350
Maprs587782350
PheGenIrs587782350
hapmaprs587782350
1000 genomesrs587782350
hgdprs587782350
ensemblrs587782350
gopubmedrs587782350
geneviewrs587782350
scholarrs587782350
googlers587782350
pharmgkbrs587782350
gwascentralrs587782350
openSNPrs587782350
23andMers587782350
23andMe allrs587782350
SNP Nexus

SNPshotrs587782350
SNPdbers587782350
MSV3drs587782350
GWAS Ctlgrs587782350
Max Magnitude0
ClinVar
Risk rs587782350(T;T)
Alt rs587782350(T;T)
Reference rs587782350(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89717712C>T
CLNSRC
CLNACC RCV000131292.4, RCV000212883.1,