C0267662[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 55964	NM_000111.3(SLC26A3):c.1136G>C (p.Gly379Ala)	SLC26A3 (G379A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 911310	NM_000111.3(SLC26A3):c.455G>A (p.Arg152His)	SLC26A3 (R152H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 55997	NM_000111.3(SLC26A3):c.358G>A (p.Gly120Ser)	SLC26A3 (G120S)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic

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