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

rs1064796078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome10
Position87864515
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs1064796078
dbSNP (old)rs1064796078
ClinGenrs1064796078
ebirs1064796078
HLIrs1064796078
Exacrs1064796078
Gnomadrs1064796078
Varsomers1064796078
Maprs1064796078
PheGenIrs1064796078
Biobankrs1064796078
1000 genomesrs1064796078
hgdprs1064796078
ensemblrs1064796078
gopubmedrs1064796078
geneviewrs1064796078
scholarrs1064796078
googlers1064796078
pharmgkbrs1064796078
gwascentralrs1064796078
openSNPrs1064796078
23andMers1064796078
23andMe allrs1064796078
SNPshotrs1064796078
SNPdbers1064796078
MSV3drs1064796078
GWAS Ctlgrs1064796078
Max Magnitude0
ClinVar
Risk rs1064796078(C;C) rs1064796078(G;G)
Alt rs1064796078(C;C) rs1064796078(G;G)
Reference Rs1064796078(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PTEN KLLN
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000010.10:g.89624272T>C; NC_000010.10:g.89624272T>G
CLNSRC
CLNACC RCV000491437.1, RCV000481194.1,