| | | Single nucleotide variant (nonsense +1 more) | Intellectual disability, autosomal recessive 47 | |
| | | Deletion (frameshift variant +1 more) | Intellectual disability, autosomal recessive 47 | |
| | | Copy number loss | not specified | |
| | | Single nucleotide variant (nonsense) | Intellectual disability, autosomal recessive 47 | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal recessive 47 | |
| | FMN2, LOC126806069 (M1376I +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FMN2, LOC126806069 (H1384Y +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | FMN2, LOC126806069 (V1356L +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal recessive 47 | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal recessive 47 | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal recessive 47 | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal recessive 47 | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal recessive 47 | |
| | FMN2, LOC126806069 (K1367R +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Intellectual disability, autosomal recessive 47 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability, autosomal recessive 47 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability | |
| | | Single nucleotide variant (missense variant +1 more) | Intellectual disability | |
| | | Single nucleotide variant (intron variant) | Intellectual disability | |
| | | Single nucleotide variant (missense variant) | Intellectual disability | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Copy number loss | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | FMN2, LOC126806069 (L1379I +2 more) | Single nucleotide variant (missense variant) | not provided +2 more | |