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rs786204928

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204928(C;T)
Make rs786204928(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933048
GenePTEN
is asnp
is mentioned by
dbSNPrs786204928
ebirs786204928
HLIrs786204928
Exacrs786204928
Varsomers786204928
Maprs786204928
PheGenIrs786204928
hapmaprs786204928
1000 genomesrs786204928
hgdprs786204928
ensemblrs786204928
gopubmedrs786204928
geneviewrs786204928
scholarrs786204928
googlers786204928
pharmgkbrs786204928
gwascentralrs786204928
openSNPrs786204928
23andMers786204928
23andMe allrs786204928
SNP Nexus

SNPshotrs786204928
SNPdbers786204928
MSV3drs786204928
GWAS Ctlgrs786204928
Max Magnitude0
ClinVar
Risk rs786204928(T;T)
Alt rs786204928(T;T)
Reference rs786204928(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692805C>T
CLNSRC
CLNACC RCV000169873.1,