C0342739[trait identifier] AND "Hehr Laboratory, Center for Human Gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 562008	NM_001002294.3(FMO3):c.370C>T (p.Gln124Ter)	LOC126805916, FMO3 (Q124* +2 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 562009	NM_001002294.3(FMO3):c.442G>A (p.Gly148Arg)	FMO3, LOC126805916 (G148R +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GLikely pathogenic