C3810055[trait identifier] AND "Mayo Clinic Laboratories, Mayo Clinic" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 380035	NM_020408.6(LYRM4):c.31T>G (p.Ser11Ala)	FARS2, LOC129995672 +1 more (S11A)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 547901	NM_020408.6(LYRM4):c.7G>A (p.Ala3Thr)	FARS2, LOC129995672 +1 more (A3T)	Single nucleotide variant (missense variant +1 more)	Combined oxidative phosphorylation deficiency 19	GUncertain significance