| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | JAK2, INSL6 (L393V +1 more) | Single nucleotide variant (missense variant +2 more) | not provided | GConflicting classifications of pathogenicity |
| | INSL6, JAK2 (G516fs +2 more) | Duplication (frameshift variant +1 more) | not provided | |
| | INSL6, JAK2 (N273T +2 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | INSL6, JAK2 (S350R +2 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | INSL6, JAK2 (L425V +2 more) | Indel (missense variant +1 more) | not provided | |
| | INSL6, JAK2 (T483S +2 more) | Single nucleotide variant (missense variant +1 more) | not provided | GConflicting classifications of pathogenicity |
| | INSL6, JAK2 (N1108S +2 more) | Single nucleotide variant (missense variant +1 more) | not specified +2 more | GConflicting classifications of pathogenicity |
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