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rs398123325

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123325(A;A)
Make rs398123325(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87933222
GenePTEN
is asnp
is mentioned by
dbSNPrs398123325
ebirs398123325
HLIrs398123325
Exacrs398123325
Varsomers398123325
Maprs398123325
PheGenIrs398123325
hapmaprs398123325
1000 genomesrs398123325
hgdprs398123325
ensemblrs398123325
gopubmedrs398123325
geneviewrs398123325
scholarrs398123325
googlers398123325
pharmgkbrs398123325
gwascentralrs398123325
openSNPrs398123325
23andMers398123325
23andMe allrs398123325
SNP Nexus

SNPshotrs398123325
SNPdbers398123325
MSV3drs398123325
GWAS Ctlgrs398123325
Max Magnitude0
ClinVar
Risk rs398123325(A;A)
Alt rs398123325(A;A)
Reference rs398123325(T;T)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692979T>A
CLNSRC
CLNACC RCV000078619.3, RCV000169798.1,