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rs1064794993

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position41346919
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1064794993
dbSNP (classic)rs1064794993
ClinGenrs1064794993
ebirs1064794993
HLIrs1064794993
Exacrs1064794993
Gnomadrs1064794993
Varsomers1064794993
LitVarrs1064794993
Maprs1064794993
PheGenIrs1064794993
Biobankrs1064794993
1000 genomesrs1064794993
hgdprs1064794993
ensemblrs1064794993
geneviewrs1064794993
scholarrs1064794993
googlers1064794993
pharmgkbrs1064794993
gwascentralrs1064794993
openSNPrs1064794993
23andMers1064794993
SNPshotrs1064794993
SNPdbers1064794993
MSV3drs1064794993
GWAS Ctlgrs1064794993
Max Magnitude0
ClinVar
Risk rs1064794993(A;A)
Alt rs1064794993(A;A)
Reference Rs1064794993(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41206172T>A
CLNSRC
CLNACC RCV000482989.1,