"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CD55"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 787220	NM_000574.5(CD55):c.155G>T (p.Arg52Leu)	CD55 (R52L)	Single nucleotide variant (missense variant +1 more)	CD55-related condition +3 more	GBenign/Likely benign
Select item 1066401	NM_000574.5(CD55):c.286+2T>G	CD55	Single nucleotide variant (splice donor variant)	not provided +2 more	GLikely pathogenic
Select item 1346393	NM_000574.5(CD55):c.1081+1G>C	CD55	Single nucleotide variant (splice donor variant)	Protein-losing enteropathy +2 more	GUncertain significance

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