| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (L675V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (L695F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (F696C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3-AS1, CACNA2D3 (V700A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3-AS1, CACNA2D3 (G729S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (L739P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (F740L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (Q745E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (D756N) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CACNA2D3, CACNA2D3-AS1 (D808N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CACNA2D3, LRTM1 (I215T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CACNA2D3, LRTM1 (R207H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LRTM1, CACNA2D3 (L119V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LRTM1, CACNA2D3 (A164V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CACNA2D3, LRTM1 (L161P +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LRTM1, CACNA2D3 (I150V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CACNA2D3, LRTM1 (L51F +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CACNA2D3, LRTM1 (E126G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | CACNA2D3, LRTM1 (N7I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |