DLX3, distal-less homeobox 3, 1747

N. diseases: 67; N. variants: 5
Disease: Taurodontism ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057518764
rs1057518764 		0.827 0.200 17 49991807 frameshift variant C/-;CC delins
CUI: C0266039
Disease: Taurodontism
Taurodontism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases 0.700 0
dbSNP: rs1555617226
rs1555617226 		0.851 0.160 17 49993440 missense variant C/A snv
CUI: C0266039
Disease: Taurodontism
Taurodontism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases 0.700 0