| | LOC130006930, LOC130006931 +1199 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129390375, LOC129390376 +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 | |
| | LOC130007028, LOC130007029 +608 more | Duplication | Schizophrenia | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129390377, LOC129390378 +488 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC130007011, LOC130007012 +440 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC130007071, LOC130007072 +363 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC112061823, LOC112067710 +352 more | Copy number loss | See cases | |
| | TMEM218, TMEM45B +343 more | Copy number loss | See cases | |
| | LOC130007029, LOC130007030 +312 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 | |
| | LOC121392949, LOC121392950 +261 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 | |
| | ADAMTS15, ADAMTS8 +99 more | Copy number loss | See cases | |
| | | Microsatellite (5 prime UTR variant) | Congenital long QT syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | GConflicting classifications of pathogenicity |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | GConflicting classifications of pathogenicity |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | GConflicting classifications of pathogenicity |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Microsatellite (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Familial hyperaldosteronism +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Familial hyperaldosteronism +2 more | GConflicting classifications of pathogenicity |
| | | Insertion (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Deletion (5 prime UTR variant) | not provided | |
| | | Deletion (5 prime UTR variant) | Familial hyperaldosteronism +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +3 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Deletion (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Deletion (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Long QT syndrome 13 +1 more | |
| | | Microsatellite (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Microsatellite (5 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Microsatellite (5 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Indel (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Insertion (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | |
| | | Deletion (5 prime UTR variant) | Familial hyperaldosteronism +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial hyperaldosteronism type III | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |