| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126807485, SEMA6A (R237G) | Single nucleotide variant (missense variant) | not specified | |
| | SEMA6A, SEMA6A-AS1 (R677Q +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | SEMA6A, SEMA6A-AS1 (V633L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | SEMA6A, SEMA6A-AS1 (P618H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | SEMA6A, SEMA6A-AS1 (R713W +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | SEMA6A, SEMA6A-AS1 (H642Q +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC126807485, SEMA6A (G229A) | Single nucleotide variant (missense variant) | not specified | |
| | SEMA6A, SEMA6A-AS1 (W606R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | SEMA6A, SEMA6A-AS1 (S591L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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