"Baylor Genetics"[submitter] AND "C4A"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1029153	NM_007293.3(C4A):c.3059C>T (p.Pro1020Leu)	C4A (P1020L)	Single nucleotide variant (missense variant)	Complement component 4a deficiency	GUncertain significance
Select item 1034372	NM_007293.3(C4A):c.3453T>G (p.His1151Gln)	C4A (H1151Q)	Single nucleotide variant (missense variant)	Complement component 4a deficiency	GUncertain significance
Select item 625706	GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367)	ERVH-3, ETV7 +427 more	Copy number gain	not provided	GPathogenic

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