C3280378[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 1163413	NM_212552.3(BOLA3):c.296G>A (p.Arg99Gln)	BOLA3 (R99Q)	Single nucleotide variant (synonymous variant +1 more)	Multiple mitochondrial dysfunctions syndrome 2 +2 more	GUncertain significance
Select item 214169	NM_212552.3(BOLA3):c.45G>T (p.Gly15=)	BOLA3	Single nucleotide variant (synonymous variant)	BOLA3-related condition +3 more	GBenign/Likely benign