| | LOC132088675, LOC132088682 +1585 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126805925, LOC126805926 +239 more | Copy number loss | See cases | |
| | LOC122149328, LOC122149329 +540 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (5 prime UTR variant) | Trimethylaminuria | |
| | | Single nucleotide variant (splice acceptor variant) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Deletion (frameshift variant +1 more) | not provided | |
| | | Deletion (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | FMO3-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Trimethylaminuria | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Duplication (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Trimethylaminuria | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | FMO3-related condition | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Trimethylaminuria | |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Insertion (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Trimethylaminuria | |
| | | Deletion (frameshift variant +1 more) | Trimethylaminuria | |
| | | Single nucleotide variant (missense variant +1 more) | Trimethylaminuria | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Trimethylaminuria +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Trimethylaminuria | |
| | | Single nucleotide variant (missense variant +1 more) | Trimethylaminuria | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (splice donor variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Microsatellite (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Trimethylaminuria +3 more | GConflicting classifications of pathogenicity |
| | FMO3, LOC126805916 (A57fs +2 more) | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126805916, FMO3 (Q124* +2 more) | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | FMO3, LOC126805916 (R131fs +2 more) | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (D132H +2 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | FMO3, LOC126805916 (E73* +2 more) | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (V123E +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria | |
| | FMO3, LOC126805916 (M144V +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | FMO3, LOC126805916 (G148R +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria | |
| | FMO3, LOC126805916 (G148* +2 more) | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (P153L +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (V187A +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | FMO3, LOC126805916 (E308G +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Trimethylaminuria | |
| | | Single nucleotide variant (intron variant) | Trimethylaminuria +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | FMO3, LOC126805916 (L100fs +2 more) | Deletion (frameshift variant) | not provided | |
| | FMO3, LOC126805916 (C107W +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (E115fs +2 more) | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (G160V +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (V124fs +2 more) | Deletion (frameshift variant) | not provided | |
| | FMO3, LOC126805916 (V124G +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FMO3, LOC126805916 (V187A +2 more) | Single nucleotide variant (missense variant) | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FMO3, LOC126805916 (S195* +2 more) | Single nucleotide variant (nonsense) | not provided | |
| | FMO3, LOC126805916 (S132L +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Microsatellite (nonsense) | Trimethylaminuria +1 more | |
| | FMO3, LOC126805916 (D178E +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | FMO3, LOC126805916 (T138P +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria | |
| | FMO3, LOC126805916 (R142C +2 more) | Single nucleotide variant (missense variant) | Trimethylaminuria +2 more | GConflicting classifications of pathogenicity |
| | FMO3, LOC126805916 (E145* +2 more) | Single nucleotide variant (nonsense) | Trimethylaminuria +1 more | |
| | FMO3, LOC126805916 (Q146* +2 more) | Single nucleotide variant (nonsense) | not provided | |