DLX3, distal-less homeobox 3, 1747

N. diseases: 67; N. variants: 5
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: C0266039
Disease:
Taurodontism
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0265333
Disease:
Tricho-dento-osseous syndrome (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0345030
Disease:
Peripheral pulmonary artery stenosis
TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0157733
Disease:
Abnormality of the hair
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0002452
Disease:
Amelogenesis Imperfecta
TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C1863012
Disease:
Amelogenesis Imperfecta, Type IV
T 0.700 CausalMutation CLINVAR
dbSNP: rs1057518764
rs1057518764
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0002452
Disease:
Amelogenesis Imperfecta
T 0.700 CausalMutation CLINVAR
dbSNP: rs1555617226
rs1555617226
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0265333
Disease:
Tricho-dento-osseous syndrome (disorder)
A 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: rs1555617226
rs1555617226
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0266039
Disease:
Taurodontism
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555617226
rs1555617226
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0002452
Disease:
Amelogenesis Imperfecta
A 0.700 CausalMutation CLINVAR
dbSNP: rs387906405
rs387906405
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0265333
Disease:
Tricho-dento-osseous syndrome (disorder)
T 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
dbSNP: rs387906406
rs387906406
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0265333
Disease:
Tricho-dento-osseous syndrome (disorder)
T 0.700 CausalMutation CLINVAR
dbSNP: rs2278163
rs2278163
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0011334
Disease:
Dental caries
0.020 GeneticVariation BEFREE The aim of this study was to analyze the association between BMP2 (rs1884302) and DLX3 (rs2278163) gene polymorphisms and dental caries in primary and permanent dentitions. 29059672 2018
dbSNP: rs2278163
rs2278163
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0011334
Disease:
Dental caries
0.020 GeneticVariation BEFREE T and C alleles of rs2278163 SNP may potentially be involved in caries susceptibility and caries protection respectively. 25247779 2015
dbSNP: rs2278163
rs2278163
Entrez Id: 1747
Gene Symbol: DLX3
DLX3
CUI: C0333519
Disease:
Caries (morphologic abnormality)
0.010 GeneticVariation BEFREE T and C alleles of rs2278163 SNP may potentially be involved in caries susceptibility and caries protection respectively. 25247779 2015