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

rs1057518707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518707(A;A)
Make rs1057518707(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41345206
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1057518707
dbSNP (old)rs1057518707
ClinGenrs1057518707
ebirs1057518707
HLIrs1057518707
Exacrs1057518707
Gnomadrs1057518707
Varsomers1057518707
Maprs1057518707
PheGenIrs1057518707
Biobankrs1057518707
1000 genomesrs1057518707
hgdprs1057518707
ensemblrs1057518707
gopubmedrs1057518707
geneviewrs1057518707
scholarrs1057518707
googlers1057518707
pharmgkbrs1057518707
gwascentralrs1057518707
openSNPrs1057518707
23andMers1057518707
23andMe allrs1057518707
SNPshotrs1057518707
SNPdbers1057518707
MSV3drs1057518707
GWAS Ctlgrs1057518707
Max Magnitude0
ClinVar
Risk rs1057518707(A;A)
Alt rs1057518707(A;A)
Reference Rs1057518707(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41204459G>A
CLNSRC
CLNACC RCV000414932.1,