Related gene-specific medical variations for Gene (Select 2329) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3064094	NM_002022.3(FMO4):c.83C>A (p.Pro28His)	FMO4 (P28H)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 1340726	GRCh37/hg19 1q24.3(chr1:171294383-171371123)x1	FMO4	Copy number loss	not provided	GLikely benign
Select item 565196	GRCh37/hg19 1q24.3(chr1:171294057-171376751)x1	FMO4	Copy number loss	not provided	GLikely benign

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