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rs786204875

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204875(A;A)
Make rs786204875(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87960913
GenePTEN
is asnp
is mentioned by
dbSNPrs786204875
ebirs786204875
HLIrs786204875
Exacrs786204875
Varsomers786204875
Maprs786204875
PheGenIrs786204875
hapmaprs786204875
1000 genomesrs786204875
hgdprs786204875
ensemblrs786204875
gopubmedrs786204875
geneviewrs786204875
scholarrs786204875
googlers786204875
pharmgkbrs786204875
gwascentralrs786204875
openSNPrs786204875
23andMers786204875
23andMe allrs786204875
SNP Nexus

SNPshotrs786204875
SNPdbers786204875
MSV3drs786204875
GWAS Ctlgrs786204875
Max Magnitude0
ClinVar
Risk rs786204875(A;A)
Alt rs786204875(A;A)
Reference rs786204875(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.89720670G>A
CLNSRC
CLNACC RCV000169815.1,