"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CHST3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 776518	NM_004273.5(CHST3):c.108C>G (p.Val36=)	CHST3	Single nucleotide variant (synonymous variant)	Spondyloepiphyseal dysplasia with congenital joint dislocations +1 more	GBenign/Likely benign
Select item 196377	NM_004273.5(CHST3):c.1173C>A (p.Ile391=)	CHST3	Single nucleotide variant (synonymous variant)	Spondyloepiphyseal dysplasia with congenital joint dislocations +3 more	GBenign/Likely benign