Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777318
rs587777318
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C3806746
Disease:
MENTAL RETARDATION, X-LINKED 99 		C 0.700 CausalMutation CLINVAR
dbSNP: rs869025588
rs869025588
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C4225416
Disease:
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED 		T 0.700 CausalMutation CLINVAR
dbSNP: rs869025589
rs869025589
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C4225416
Disease:
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED 		G 0.700 CausalMutation CLINVAR
dbSNP: rs869025590
rs869025590
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C4225416
Disease:
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED 		CA 0.700 CausalMutation CLINVAR
dbSNP: rs869025591
rs869025591
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C4225416
Disease:
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED 		T 0.700 CausalMutation CLINVAR
dbSNP: rs869025592
rs869025592
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C4225416
Disease:
MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED 		T 0.700 CausalMutation CLINVAR
dbSNP: rs587777317
rs587777317
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C3806746
Disease:
MENTAL RETARDATION, X-LINKED 99 		0.800 GeneticVariation UNIPROT Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth. 24607389 2014
dbSNP: rs587777317
rs587777317
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C3806746
Disease:
MENTAL RETARDATION, X-LINKED 99 		A 0.800 CausalMutation CLINVAR