| | ADAM15, ADAM15-EFNA4 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | ADAM15, ADAM15-EFNA4 +1 more (Q635P +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (H521R +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (C685R +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15-EFNA4, DCST1-AS1 +1 more (I346V +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R724Q +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R380Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (E412K +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (M390K +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (C750R +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (L137P +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (A543V +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (D588V +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (E52K +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R116Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (M317V +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R718H +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R795H +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (P749L +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R252H +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (Q697K +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R184C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (L386I +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +2 more (L18P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R168W +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R645Q +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (P475L +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (L746I +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (P766L +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +2 more (P19S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (P769T +1 more) | Single nucleotide variant (synonymous variant +3 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (N373T +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (P777L +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +2 more (A4T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (E417K +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (A552T +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (R756G +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (K69E +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (M411V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (I587T +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (G111E +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (A331S +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (V128I +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more (H80Y +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ADAM15, ADAM15-EFNA4 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | ADAM15, ADAM15-EFNA4 +1 more (L224M +2 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | ADAM15, ADAM15-EFNA4 +1 more (P745L) | Single nucleotide variant (missense variant +3 more) | not provided | |