Have questions? Visit https://www.reddit.com/r/SNPedia

rs121913289

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913289(-;-)
Make rs121913289(-;A)
ReferenceGRCh38 38.1/141
Chromosome10
Position87958018
GenePTEN
is asnp
is mentioned by
dbSNPrs121913289
ebirs121913289
HLIrs121913289
Exacrs121913289
Varsomers121913289
Maprs121913289
PheGenIrs121913289
hapmaprs121913289
1000 genomesrs121913289
hgdprs121913289
ensemblrs121913289
gopubmedrs121913289
geneviewrs121913289
scholarrs121913289
googlers121913289
pharmgkbrs121913289
gwascentralrs121913289
openSNPrs121913289
23andMers121913289
23andMe allrs121913289
SNP Nexus

SNPshotrs121913289
SNPdbers121913289
MSV3drs121913289
GWAS Ctlgrs121913289
Max Magnitude0
ClinVar
Risk rs121913289(;)
Alt rs121913289(;)
Reference rs121913289(A;A)
Significance Pathogenic
Disease not provided PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN not provided PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89717775delA
CLNSRC HGMD
CLNACC RCV000078622.3, RCV000231858.1,