| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | LMNB2, LOC130063066 (A18V) | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Indel (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | LMNB2, LOC130063066 (R14G) | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +2 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly 27, primary, autosomal dominant +1 more | |
| | | Duplication | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (intron variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | LMNB2, LOC130063065 (R87H) | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Microsatellite (intron variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | LMNB2-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (missense variant) | Lipodystrophy, partial, acquired, susceptibility to +2 more | |
| | | Single nucleotide variant (missense variant) | Progressive myoclonic epilepsy type 9 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Lipodystrophy, partial, acquired, susceptibility to +1 more | |