| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861443, MFAP5 (R136L +4 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
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