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rs786204858

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204858(A;G)
Make rs786204858(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87933079
GenePTEN
is asnp
is mentioned by
dbSNPrs786204858
ebirs786204858
HLIrs786204858
Exacrs786204858
Varsomers786204858
Maprs786204858
PheGenIrs786204858
hapmaprs786204858
1000 genomesrs786204858
hgdprs786204858
ensemblrs786204858
gopubmedrs786204858
geneviewrs786204858
scholarrs786204858
googlers786204858
pharmgkbrs786204858
gwascentralrs786204858
openSNPrs786204858
23andMers786204858
23andMe allrs786204858
SNP Nexus

SNPshotrs786204858
SNPdbers786204858
MSV3drs786204858
GWAS Ctlgrs786204858
Max Magnitude0
ClinVar
Risk rs786204858(G;G)
Alt rs786204858(G;G)
Reference rs786204858(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89692836A>G
CLNSRC
CLNACC RCV000169796.1,