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rs398123321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123321(C;C)
Make rs398123321(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87933090
GenePTEN
is asnp
is mentioned by
dbSNPrs398123321
ebirs398123321
HLIrs398123321
Exacrs398123321
Varsomers398123321
Maprs398123321
PheGenIrs398123321
hapmaprs398123321
1000 genomesrs398123321
hgdprs398123321
ensemblrs398123321
gopubmedrs398123321
geneviewrs398123321
scholarrs398123321
googlers398123321
pharmgkbrs398123321
gwascentralrs398123321
openSNPrs398123321
23andMers398123321
23andMe allrs398123321
SNP Nexus

SNPshotrs398123321
SNPdbers398123321
MSV3drs398123321
GWAS Ctlgrs398123321
Max Magnitude0
ClinVar
Risk rs398123321(C;C)
Alt rs398123321(C;C)
Reference rs398123321(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692847T>C
CLNSRC HGMD
CLNACC RCV000078613.4,