| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Copy number gain | See cases | |
| | FADS2, LOC130005809
+1 more | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | FADS1, FADS2
+1 more (P39R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | FADS1, FADS2
+1 more (R28H) | Single nucleotide variant (missense variant +1 more) | not specified | |
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