"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CRELD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1605652	NM_001077415.3(CRELD1):c.258-13C>A	CRELD1	Single nucleotide variant (intron variant)	Atrioventricular septal defect, susceptibility to, 2	GBenign/Likely benign
Select item 841606	NM_001077415.3(CRELD1):c.796dup (p.Glu266fs)	CRELD1 (E266fs)	Duplication (frameshift variant +2 more)	not provided +1 more	GUncertain significance