C1848097[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 774542	NM_001711.6(BGN):c.111C>T (p.Asn37=)	BGN	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 1098726	NM_001711.6(BGN):c.257A>G (p.Lys86Arg)	BGN (K86R)	Single nucleotide variant (missense variant)	X-linked spondyloepimetaphyseal dysplasia +4 more	GBenign/Likely benign
Select item 1316894	NM_001711.6(BGN):c.954C>T (p.Asn318=)	BGN	Single nucleotide variant (synonymous variant)	not provided +3 more	GLikely benign

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