| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130057537, SEMA7A (P5L) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | SEMA7A-related disorder | |
| | | Single nucleotide variant (synonymous variant) | SEMA7A-related disorder | |
| | LOC130057537, SEMA7A (P21L) | Single nucleotide variant (missense variant) | not specified | |
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