| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129936377, LOC129936378 +1111 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129936460, LOC129936461 +176 more | Copy number gain | See cases | |
| | | Deletion | Brugada syndrome | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | ITGA9-related condition | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | ITGA9-related condition | |
| | | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene