C3809383[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 424440	NM_007074.4(CORO1A):c.1189G>A (p.Val397Ile)	CORO1A (V397I)	Single nucleotide variant (missense variant)	Severe combined immunodeficiency due to CORO1A deficiency +2 more	GConflicting classifications of pathogenicity
Select item 953260	NM_007074.4(CORO1A):c.1237G>A (p.Gly413Arg)	CORO1A (G413R)	Single nucleotide variant (missense variant)	Severe combined immunodeficiency due to CORO1A deficiency +2 more	GUncertain significance