| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (E103G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (W115R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (L121V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (L121R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (W143G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (R147Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (G160D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (I167F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FUT4, LOC130006601 (W172L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |