C3809845[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 668223	NM_013352.4(DSE):c.216G>A (p.Thr72=)	DSE	Single nucleotide variant (synonymous variant +2 more)	DSE-related disorder +2 more	GBenign/Likely benign
Select item 515381	NM_013352.4(DSE):c.240C>T (p.Ser80=)	DSE	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 668224	NM_013352.4(DSE):c.2651G>A (p.Arg884Gln)	DSE (R903Q +4 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GLikely benign

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