Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853272
rs137853272
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		0.800 GeneticVariation UNIPROT Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. 17668385 2007
dbSNP: rs137853272
rs137853272
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		C 0.800 CausalMutation CLINVAR
dbSNP: rs28417201
rs28417201
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs1057518650
rs1057518650
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1569290395
rs1569290395
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs730882185
rs730882185
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs730882186
rs730882186
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		CT 0.700 CausalMutation CLINVAR
dbSNP: rs863224851
rs863224851
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3
CUI: C1970841
Disease:
MENTAL RETARDATION, X-LINKED 93 (disorder) 		C 0.700 GeneticVariation CLINVAR