C5551343[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 703755	NM_183357.3(ADCY5):c.3375C>T (p.Ile1125=)	ADCY5	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 1165394	NM_183357.3(ADCY5):c.3064-18G>A	ADCY5	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 697428	NM_183357.3(ADCY5):c.2481C>A (p.Ile827=)	ADCY5	Single nucleotide variant (synonymous variant)	Dyskinesia with orofacial involvement, autosomal recessive +3 more	GBenign/Likely benign
Select item 1031781	NM_183357.3(ADCY5):c.400G>A (p.Gly134Ser)	ADCY5 (G134S)	Single nucleotide variant (missense variant)	Dyskinesia with orofacial involvement, autosomal dominant +4 more	GConflicting classifications of pathogenicity
Select item 390053	NM_183357.3(ADCY5):c.304G>A (p.Ala102Thr)	ADCY5 (A102T)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1165864	NM_183357.3(ADCY5):c.242C>T (p.Pro81Leu)	ADCY5 (P81L)	Single nucleotide variant (missense variant)	Dyskinesia with orofacial involvement, autosomal dominant +3 more	GConflicting classifications of pathogenicity
Select item 702084	NM_183357.3(ADCY5):c.130C>T (p.His44Tyr)	ADCY5 (H44Y)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign

ClinVar