| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC112872301, PLXND1 (D1784G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112872301, PLXND1 (I1775F) | Single nucleotide variant (missense variant) | Congenital heart defects, multiple types, 9 | |
| | LOC112872301, PLXND1 (I1775V) | Single nucleotide variant (missense variant) | not specified | |
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