C0342739[trait identifier] AND "Mendelics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 875849	NM_001002294.3(FMO3):c.341A>G (p.Asn114Ser)	FMO3 (N114S +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +3 more	GConflicting classifications of pathogenicity
Select item 38395	NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly)	FMO3 (E308G +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign