C3280642[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1029153	NM_001242823.2(C4B_2):c.3059C>T (p.Pro1020Leu)	C4A (P1020L)	Single nucleotide variant (missense variant)	Complement component 4a deficiency	GUncertain significance
Select item 1034372	NM_001242823.2(C4B_2):c.3453T>G (p.His1151Gln)	C4A (H1151Q)	Single nucleotide variant (missense variant)	Complement component 4a deficiency	GUncertain significance