"Fulgent Genetics, Fulgent Genetics"[submitter] AND "C8A"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1164179	NM_000562.3(C8A):c.107C>A (p.Ala36Glu)	C8A (A36E)	Single nucleotide variant (missense variant)	Type I complement component 8 deficiency +1 more	GBenign
Select item 791416	NM_000562.3(C8A):c.606T>C (p.Asp202=)	C8A	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 789429	NM_000562.3(C8A):c.1331G>A (p.Arg444His)	C8A (R444H)	Single nucleotide variant (missense variant)	Type I complement component 8 deficiency +1 more	GLikely benign

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