| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (intron variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (intron variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (intron variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (intron variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (nonsense) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (intron variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (nonsense) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (missense variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (intron variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA3E-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (synonymous variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (intron variant) | CHARGE syndrome | |
| | | Single nucleotide variant (synonymous variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (intron variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (synonymous variant) | CHARGE syndrome | |
| | | Single nucleotide variant (synonymous variant) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |
| | | Single nucleotide variant (nonsense) | CHARGE syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | CHARGE syndrome | |
| | | Single nucleotide variant (missense variant) | CHARGE syndrome | |