| | LMNA, LOC126805877 (E145K +2 more) | Single nucleotide variant (missense variant) | Hutchinson-Gilford progeria syndrome, atypical | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Deletion (splice acceptor variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (missense variant) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Primary dilated cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hutchinson-Gilford progeria syndrome, atypical | |
| | | Single nucleotide variant (splice donor variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (splice donor variant +1 more) | Hutchinson-Gilford syndrome +1 more | |
| | | Single nucleotide variant (splice donor variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (intron variant +1 more) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (intron variant) | Hutchinson-Gilford syndrome | |
| | | Single nucleotide variant (intron variant) | Hutchinson-Gilford syndrome | |