| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FGD5, LOC126806615 (A1266T) | Single nucleotide variant (missense variant) | not specified | |
| | FGD5, LOC126806615 (E1299D) | Single nucleotide variant (missense variant) | not specified | |
| | FGD5, LOC126806615 (S1231G) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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