C4082304[trait identifier] AND "Department of Prosthodontics, School a - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 986783	NM_022336.4(EDAR):c.338G>A (p.Cys113Tyr)	EDAR, RANBP2 (C113Y)	Single nucleotide variant (missense variant)	Oligodontia	GPathogenic
Select item 1064708	NM_002448.3(MSX1):c.576_577insTAG (p.Gln193Ter)	MSX1 (Q193*)	Insertion (nonsense)	Oligodontia	GPathogenic
Select item 1064705	NM_001372076.1(PAX9):c.140G>C (p.Arg47Pro)	PAX9 (R47P)	Single nucleotide variant (missense variant)	Oligodontia	GPathogenic
Select item 1064704	NM_001372076.1(PAX9):c.146C>T (p.Ser49Leu)	PAX9 (S49L)	Single nucleotide variant (missense variant)	Oligodontia	GPathogenic
Select item 1119978	NM_001372076.1(PAX9):c.152G>T (p.Gly51Val)	PAX9 (G51V)	Single nucleotide variant (missense variant)	Oligodontia	GPathogenic
Select item 1064706	NM_001372076.1(PAX9):c.243del (p.Thr82fs)	PAX9 (T82fs)	Deletion (frameshift variant)	Oligodontia	GPathogenic
Select item 1064707	NM_001372076.1(PAX9):c.409C>T (p.Gln137Ter)	PAX9 (Q137*)	Single nucleotide variant (nonsense)	Oligodontia	GPathogenic

ClinVar