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rs786204934

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204934(G;T)
Make rs786204934(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933207
GenePTEN
is asnp
is mentioned by
dbSNPrs786204934
ebirs786204934
HLIrs786204934
Exacrs786204934
Varsomers786204934
Maprs786204934
PheGenIrs786204934
hapmaprs786204934
1000 genomesrs786204934
hgdprs786204934
ensemblrs786204934
gopubmedrs786204934
geneviewrs786204934
scholarrs786204934
googlers786204934
pharmgkbrs786204934
gwascentralrs786204934
openSNPrs786204934
23andMers786204934
23andMe allrs786204934
SNP Nexus

SNPshotrs786204934
SNPdbers786204934
MSV3drs786204934
GWAS Ctlgrs786204934
Max Magnitude0
ClinVar
Risk rs786204934(T;T)
Alt rs786204934(T;T)
Reference rs786204934(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692964G>T
CLNSRC
CLNACC RCV000169879.1,