| | LOC130006930, LOC130006931 +1199 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130007012, LOC130007013 +769 more | Copy number gain | See cases | |
| | LOC126861364, LOC126861365 +764 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130007028, LOC130007029 +608 more | Duplication | Schizophrenia | |
| | LOC130006995, LOC130006996 +551 more | Copy number loss | See cases | |
| | LOC121832824, LOC124625855 +549 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126861375, LOC126861376 +444 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Duplication | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome | |
| | | Microsatellite (3 prime UTR variant) | Brugada syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome | |
| | | Microsatellite (3 prime UTR variant) | Brugada syndrome | |
| | | Duplication (3 prime UTR variant) | Brugada syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Brugada syndrome | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Duplication (frameshift variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Sudden cardiac death | |
| | | Single nucleotide variant (splice acceptor variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 7 | |
| | | Duplication (splice donor variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (splice donor variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 +2 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 16 | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (intron variant) | Brugada syndrome 7 | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Indel (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome 7 +3 more | |