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

rs1085308047

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position87864509
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs1085308047
dbSNP (old)rs1085308047
ClinGenrs1085308047
ebirs1085308047
HLIrs1085308047
Exacrs1085308047
Gnomadrs1085308047
Varsomers1085308047
Maprs1085308047
PheGenIrs1085308047
Biobankrs1085308047
1000 genomesrs1085308047
hgdprs1085308047
ensemblrs1085308047
gopubmedrs1085308047
geneviewrs1085308047
scholarrs1085308047
googlers1085308047
pharmgkbrs1085308047
gwascentralrs1085308047
openSNPrs1085308047
23andMers1085308047
23andMe allrs1085308047
SNPshotrs1085308047
SNPdbers1085308047
MSV3drs1085308047
GWAS Ctlgrs1085308047
Max Magnitude0
ClinVar
Risk rs1085308047(G;G)
Alt rs1085308047(G;G)
Reference Rs1085308047(A;A)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome not provided
Variation info
Gene PTEN KLLN
CLNDBN PTEN hamartoma tumor syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89624266A>G
CLNSRC
CLNACC RCV000490585.1, RCV000492940.1,