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rs1057519430

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519430(C;T)
Make rs1057519430(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41346946
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1057519430
dbSNP (old)rs1057519430
ClinGenrs1057519430
ebirs1057519430
HLIrs1057519430
Exacrs1057519430
Gnomadrs1057519430
Varsomers1057519430
Maprs1057519430
PheGenIrs1057519430
Biobankrs1057519430
1000 genomesrs1057519430
hgdprs1057519430
ensemblrs1057519430
gopubmedrs1057519430
geneviewrs1057519430
scholarrs1057519430
googlers1057519430
pharmgkbrs1057519430
gwascentralrs1057519430
openSNPrs1057519430
23andMers1057519430
23andMe allrs1057519430
SNPshotrs1057519430
SNPdbers1057519430
MSV3drs1057519430
GWAS Ctlgrs1057519430
Max Magnitude0
ClinVar
Risk rs1057519430(T;T)
Alt rs1057519430(T;T)
Reference Rs1057519430(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41206199C>T
CLNSRC
CLNACC RCV000416455.1,