| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | LOC129995898, MYLIP (A19E) | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (frameshift variant) | Coronary artery atherosclerosis | |
| | LOC129995898, MYLIP (V17A) | Single nucleotide variant (missense variant) | not provided | |
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