| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (intron variant) | THADA-related condition | |
| | | Single nucleotide variant (intron variant) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Microsatellite (inframe deletion +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Deletion (inframe deletion +2 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +2 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (intron variant) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +2 more) | THADA-related condition | |
| | LOC122757928, THADA (S1503C +2 more) | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | THADA-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Microsatellite (inframe_deletion +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | THADA, LOC122757928 (A1482V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC122757928, THADA (A1529V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Duplication | Hereditary nonpolyposis colorectal neoplasms | |
| | LOC122757928, THADA (R1496Q +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC122757928, THADA (P1582A +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |