C3809548[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 417177	NM_018076.5(ODAD2):c.2982C>T (p.Ala994=)	ODAD2	Single nucleotide variant (synonymous variant)	Primary ciliary dyskinesia +1 more	GBenign
Select item 412246	NM_018076.5(ODAD2):c.2935G>A (p.Val979Met)	ODAD2 (V979M +2 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +1 more	GConflicting classifications of pathogenicity
Select item 412251	NM_018076.5(ODAD2):c.1709G>A (p.Arg570Gln)	ODAD2 (R570Q +2 more)	Single nucleotide variant (missense variant)	Primary ciliary dyskinesia +1 more	GConflicting classifications of pathogenicity
Select item 1681375	NM_018076.5(ODAD2):c.1534-19C>G	ODAD2	Single nucleotide variant (intron variant)	Primary ciliary dyskinesia 23	GBenign/Likely benign
Select item 241257	NM_018076.5(ODAD2):c.1353T>C (p.Tyr451=)	ODAD2	Single nucleotide variant (synonymous variant +1 more)	Primary ciliary dyskinesia +2 more	GLikely benign
Select item 1253319	NM_018076.5(ODAD2):c.383-6del	ODAD2	Deletion (intron variant)	not provided +1 more	GBenign

ClinVar