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rs786204933

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204933(A;A)
Make rs786204933(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933196
GenePTEN
is asnp
is mentioned by
dbSNPrs786204933
ebirs786204933
HLIrs786204933
Exacrs786204933
Varsomers786204933
Maprs786204933
PheGenIrs786204933
hapmaprs786204933
1000 genomesrs786204933
hgdprs786204933
ensemblrs786204933
gopubmedrs786204933
geneviewrs786204933
scholarrs786204933
googlers786204933
pharmgkbrs786204933
gwascentralrs786204933
openSNPrs786204933
23andMers786204933
23andMe allrs786204933
SNP Nexus

SNPshotrs786204933
SNPdbers786204933
MSV3drs786204933
GWAS Ctlgrs786204933
Max Magnitude0
ClinVar
Risk rs786204933(A;A)
Alt rs786204933(A;A)
Reference rs786204933(T;T)
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.89692953T>A; NC_000010.10:g.89692953T>G
CLNSRC
CLNACC RCV000169878.1, RCV000198975.1,