| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Indel (missense variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Ataxia-pancytopenia syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | Monosomy 7 myelodysplasia and leukemia syndrome 1 +4 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Ataxia-pancytopenia syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder | |
| | | Deletion (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Spinocerebellar ataxia 49 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (missense variant) | Ataxia-pancytopenia syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Insertion (nonsense +1 more) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Microsatellite (inframe_deletion) | SAMD9L-related disorder +1 more | |
| | | Duplication (frameshift variant) | not provided +3 more | |
| | | Indel (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | SAMD9L-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | SAMD9L-related disorder | |