| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (stop lost +1 more) | not provided | |
| | EPHA4, LOC126806527 (R973* +1 more) | Single nucleotide variant (nonsense +1 more) | not provided | |
| | EPHA4, LOC126806527 (M972T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | EPHA4, LOC126806527 (I959V +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | EPHA4, LOC126806527 (V984L +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | EPHA4, LOC126806527 (G930V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | EPHA4, LOC126806527 (R953T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | EPHA4, LOC126806527 (T923I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | EPHA4, LOC126806527 (V986I +1 more) | Single nucleotide variant (missense variant +1 more) | EPHA4-related condition +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
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