DLX3, distal-less homeobox 3, 1747

N. diseases: 67; N. variants: 5
Disease: Amelogenesis Imperfecta, Type IV ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C1863012
Disease:
Amelogenesis Imperfecta, Type IV 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1555617226
rs1555617226
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C1863012
Disease:
Amelogenesis Imperfecta, Type IV 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387906406
rs387906406
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C1863012
Disease:
Amelogenesis Imperfecta, Type IV 		T 0.700 CausalMutation CLINVAR