| | LOC130008916, LOC130008917 +4836 more | Copy number gain | See cases | |
| | TRD-GTC2-10, TRD-GTC2-9 +906 more | Copy number gain | See cases | |
| | | Duplication (intron variant) | not provided | |
| | | Microsatellite (intron variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | TBX3-related condition | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Duplication (frameshift variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | TBX3-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | TBX3-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Deletion (frameshift variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | TBX3-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Indel (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | TBX3-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication (frameshift variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (synonymous variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | TBX3-related condition | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Deletion (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Deletion (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Duplication (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Deletion (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Microsatellite (5 prime UTR variant) | TBX3-related condition | |
| | | Insertion (5 prime UTR variant) | TBX3-related condition | |
| | | Single nucleotide variant (5 prime UTR variant) | TBX3-related condition | |
| | | Microsatellite (5 prime UTR variant) | TBX3-related condition | |
| | | Microsatellite (5 prime UTR variant) | not provided | |
| | | Microsatellite (5 prime UTR variant) | not provided +1 more | |
| | | Microsatellite (5 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Insertion (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Microsatellite (5 prime UTR variant) | Ulnar-mammary syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Ulnar-mammary syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Ulnar-mammary syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | TBX3-related condition | |
| | | Microsatellite (5 prime UTR variant) | TBX3-related condition | |
| | | Insertion (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Microsatellite (5 prime UTR variant) | Ulnar-mammary syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | TBX3-related condition | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Ulnar-mammary syndrome | |
| | LOC109286556, TBX3 +1 more | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | LOC109286556, TBX3 +1 more | Microsatellite (genic upstream transcript variant) | not provided | |