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rs786204901

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204901(-;-)
Make rs786204901(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87952210
GenePTEN
is asnp
is mentioned by
dbSNPrs786204901
ebirs786204901
HLIrs786204901
Exacrs786204901
Varsomers786204901
Maprs786204901
PheGenIrs786204901
hapmaprs786204901
1000 genomesrs786204901
hgdprs786204901
ensemblrs786204901
gopubmedrs786204901
geneviewrs786204901
scholarrs786204901
googlers786204901
pharmgkbrs786204901
gwascentralrs786204901
openSNPrs786204901
23andMers786204901
23andMe allrs786204901
SNP Nexus

SNPshotrs786204901
SNPdbers786204901
MSV3drs786204901
GWAS Ctlgrs786204901
Max Magnitude0
ClinVar
Risk rs786204901(;)
Alt rs786204901(;)
Reference rs786204901(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89711967delT
CLNSRC
CLNACC RCV000169842.1,