Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1085308039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome10
Position87933075
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308039
dbSNP (old)rs1085308039
ClinGenrs1085308039
ebirs1085308039
HLIrs1085308039
Exacrs1085308039
Gnomadrs1085308039
Varsomers1085308039
Maprs1085308039
PheGenIrs1085308039
Biobankrs1085308039
1000 genomesrs1085308039
hgdprs1085308039
ensemblrs1085308039
gopubmedrs1085308039
geneviewrs1085308039
scholarrs1085308039
googlers1085308039
pharmgkbrs1085308039
gwascentralrs1085308039
openSNPrs1085308039
23andMers1085308039
23andMe allrs1085308039
SNPshotrs1085308039
SNPdbers1085308039
MSV3drs1085308039
GWAS Ctlgrs1085308039
Max Magnitude0
ClinVar
Risk rs1085308039(T;T)
Alt rs1085308039(T;T)
Reference Rs1085308039(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692832G>T
CLNSRC
CLNACC RCV000490602.1,