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: rs765243124
rs765243124
0.827 0.160 10 104033953 frameshift variant CTCT/- delins 4.0E-06
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases 0.700 0