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rs786204871

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204871(G;G)
Make rs786204871(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87957934
GenePTEN
is asnp
is mentioned by
dbSNPrs786204871
ebirs786204871
HLIrs786204871
Exacrs786204871
Varsomers786204871
Maprs786204871
PheGenIrs786204871
hapmaprs786204871
1000 genomesrs786204871
hgdprs786204871
ensemblrs786204871
gopubmedrs786204871
geneviewrs786204871
scholarrs786204871
googlers786204871
pharmgkbrs786204871
gwascentralrs786204871
openSNPrs786204871
23andMers786204871
23andMe allrs786204871
SNP Nexus

SNPshotrs786204871
SNPdbers786204871
MSV3drs786204871
GWAS Ctlgrs786204871
Max Magnitude0
ClinVar
Risk rs786204871(G;G)
Alt rs786204871(G;G)
Reference rs786204871(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89717691T>G
CLNSRC
CLNACC RCV000169811.1,