Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518707
rs1057518707
DDX3X
0.800 GeneticVariation UNIPROT Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. 26235985

2015
dbSNP: rs1057518707
rs1057518707
DDX3X
A 0.800 CausalMutation CLINVAR Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. 26235985

2015
dbSNP: rs1057518707
rs1057518707
DDX3X
A 0.800 GeneticVariation CLINVAR