C4748855[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1258520	NM_018429.3(BDP1):c.2373-15C>T	BDP1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1028111	NM_018429.3(BDP1):c.2804G>T (p.Arg935Ile)	BDP1 (R935I)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance