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rs1064794096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position87864514
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs1064794096
dbSNP (old)rs1064794096
ClinGenrs1064794096
ebirs1064794096
HLIrs1064794096
Exacrs1064794096
Gnomadrs1064794096
Varsomers1064794096
LitVarrs1064794096
Maprs1064794096
PheGenIrs1064794096
Biobankrs1064794096
1000 genomesrs1064794096
hgdprs1064794096
ensemblrs1064794096
gopubmedrs1064794096
geneviewrs1064794096
scholarrs1064794096
googlers1064794096
pharmgkbrs1064794096
gwascentralrs1064794096
openSNPrs1064794096
23andMers1064794096
23andMe allrs1064794096
SNPshotrs1064794096
SNPdbers1064794096
MSV3drs1064794096
GWAS Ctlgrs1064794096
Max Magnitude0
ClinVar
Risk rs1064794096(C;C) rs1064794096(T;T)
Alt rs1064794096(C;C) rs1064794096(T;T)
Reference Rs1064794096(A;A)
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.89624271A>C; NC_000010.10:g.89624271A>T
CLNSRC
CLNACC RCV000491882.1, RCV000480969.1,