| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130005920, VEGFB (P18R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130005920, VEGFB (A11T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130005920, VEGFB (L10V) | Single nucleotide variant (missense variant) | not specified | |
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