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rs1064794658

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position119837773
GeneUPF3B
is asnp
is mentioned by
dbSNPrs1064794658
dbSNP (old)rs1064794658
ClinGenrs1064794658
ebirs1064794658
HLIrs1064794658
Exacrs1064794658
Gnomadrs1064794658
Varsomers1064794658
Maprs1064794658
PheGenIrs1064794658
Biobankrs1064794658
1000 genomesrs1064794658
hgdprs1064794658
ensemblrs1064794658
gopubmedrs1064794658
geneviewrs1064794658
scholarrs1064794658
googlers1064794658
pharmgkbrs1064794658
gwascentralrs1064794658
openSNPrs1064794658
23andMers1064794658
23andMe allrs1064794658
SNPshotrs1064794658
SNPdbers1064794658
MSV3drs1064794658
GWAS Ctlgrs1064794658
Max Magnitude0
ClinVar
Risk rs1064794658(G;G)
Alt rs1064794658(G;G)
Reference Rs1064794658(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UPF3B
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.118971736T>C
CLNSRC
CLNACC RCV000478703.1,