| | | Single nucleotide variant (missense variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (I55V +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (S178R +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | JAK2, INSL6 (N183S +1 more) | Single nucleotide variant (missense variant +2 more) | not specified +1 more | |
| | INSL6, JAK2 (D199H +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (H231Y +1 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (C22W +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (N646H +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | INSL6, JAK2 (G690A +2 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | INSL6, JAK2 (V314I +2 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | INSL6, JAK2 (L325I +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (T337S +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (M416I +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (P674A +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (R826K +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (R434P +2 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | INSL6, JAK2 (I494V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (E751Q +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (Q906H +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (Q550E +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (E816K +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (L621V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (L895V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (A1059V +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | INSL6, JAK2 (N1108K +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |