| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130057891, MESP2 (R83L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130057891, MESP2 (S85R) | Single nucleotide variant (missense variant) | not specified +1 more | |
| | LOC130057891, MESP2 (R99C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130057891, MESP2 (R130H) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC130057891, MESP2 (G133R) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
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