| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130064476, LTBP4 (A558P +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
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