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rs398123320

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123320(C;T)
Make rs398123320(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position87933045
GenePTEN
is asnp
is mentioned by
dbSNPrs398123320
ebirs398123320
HLIrs398123320
Exacrs398123320
Varsomers398123320
Maprs398123320
PheGenIrs398123320
hapmaprs398123320
1000 genomesrs398123320
hgdprs398123320
ensemblrs398123320
gopubmedrs398123320
geneviewrs398123320
scholarrs398123320
googlers398123320
pharmgkbrs398123320
gwascentralrs398123320
openSNPrs398123320
23andMers398123320
23andMe allrs398123320
SNP Nexus

SNPshotrs398123320
SNPdbers398123320
MSV3drs398123320
GWAS Ctlgrs398123320
Max Magnitude0
ClinVar
Risk rs398123320(T;T)
Alt rs398123320(T;T)
Reference rs398123320(C;C)
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.89692802C>T
CLNSRC
CLNACC RCV000078612.3, RCV000169794.1,