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

rs1064794133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
ChromosomeX
Position41345439
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1064794133
dbSNP (old)rs1064794133
ClinGenrs1064794133
ebirs1064794133
HLIrs1064794133
Exacrs1064794133
Gnomadrs1064794133
Varsomers1064794133
Maprs1064794133
PheGenIrs1064794133
Biobankrs1064794133
1000 genomesrs1064794133
hgdprs1064794133
ensemblrs1064794133
gopubmedrs1064794133
geneviewrs1064794133
scholarrs1064794133
googlers1064794133
pharmgkbrs1064794133
gwascentralrs1064794133
openSNPrs1064794133
23andMers1064794133
23andMe allrs1064794133
SNPshotrs1064794133
SNPdbers1064794133
MSV3drs1064794133
GWAS Ctlgrs1064794133
Max Magnitude0
ClinVar
Risk rs1064794133(-;-)
Alt rs1064794133(-;-)
Reference Rs1064794133(TCT;TCT)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41204692_41204694delCTT
CLNSRC
CLNACC RCV000480376.1,