| | | Single nucleotide variant (missense variant) | ALG9 congenital disorder of glycosylation +3 more | |
| | ATP6V0A2, LOC130009117 (M10V) | Single nucleotide variant (missense variant) | ALG9 congenital disorder of glycosylation +4 more | |
| | | Single nucleotide variant (missense variant) | ALG9 congenital disorder of glycosylation +4 more | |
| | | Single nucleotide variant (missense variant) | Wrinkly skin syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | ALG9 congenital disorder of glycosylation +4 more | |
| | | Single nucleotide variant (intron variant) | Cutis laxa with osteodystrophy +2 more | |
| | | Single nucleotide variant (missense variant) | Wrinkly skin syndrome | |
| | | Single nucleotide variant (missense variant) | Wrinkly skin syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | ALG9 congenital disorder of glycosylation +3 more | |
| | | Single nucleotide variant (intron variant) | Cutis laxa with osteodystrophy +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Cutis laxa with osteodystrophy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Wrinkly skin syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Wrinkly skin syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Wrinkly skin syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Cutis laxa with osteodystrophy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | ALG9 congenital disorder of glycosylation +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (splice donor variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Cutis laxa with osteodystrophy +1 more | |