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rs786204925

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204925(A;C)
Make rs786204925(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87931074
GenePTEN
is asnp
is mentioned by
dbSNPrs786204925
ebirs786204925
HLIrs786204925
Exacrs786204925
Varsomers786204925
Maprs786204925
PheGenIrs786204925
hapmaprs786204925
1000 genomesrs786204925
hgdprs786204925
ensemblrs786204925
gopubmedrs786204925
geneviewrs786204925
scholarrs786204925
googlers786204925
pharmgkbrs786204925
gwascentralrs786204925
openSNPrs786204925
23andMers786204925
23andMe allrs786204925
SNP Nexus

SNPshotrs786204925
SNPdbers786204925
MSV3drs786204925
GWAS Ctlgrs786204925
Max Magnitude0
ClinVar
Risk rs786204925(C;C)
Alt rs786204925(C;C)
Reference rs786204925(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89690831A>C
CLNSRC
CLNACC RCV000169870.1,