| | | Deletion (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | LOC126863275, MED12 (L480V) | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Microsatellite (inframe_insertion) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Microsatellite (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | MED12-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Duplication (inframe_insertion) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Indel (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Single nucleotide variant (missense variant) | FG syndrome | |
| | | Microsatellite (inframe_deletion) | FG syndrome | |
| | | Single nucleotide variant (synonymous variant) | FG syndrome | |
| | | Single nucleotide variant (intron variant) | FG syndrome | |