| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ELOVL6, LOC126807135 (I255V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ELOVL6, LOC126807135 (L237F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ELOVL6, LOC126807135 (V173M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ELOVL6, LOC126807135 (I128V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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