| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | FUS-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | FUS-related disorder | |
| | | Deletion (intron variant) | Amyotrophic lateral sclerosis type 6 +2 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (intron variant) | Tremor, hereditary essential, 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (missense variant +1 more) | FUS-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Microsatellite (inframe_deletion +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Tremor, hereditary essential, 4 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Tremor, hereditary essential, 4 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +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 specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +2 more) | Amyotrophic lateral sclerosis type 6 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Tremor, hereditary essential, 4 +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Tremor, hereditary essential, 4 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | FUS-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Tremor, hereditary essential, 4 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | FUS-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Indel (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Tremor, hereditary essential, 4 +1 more | |
| | | Deletion (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Insertion (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | FUS-related disorder | |
| | | Single nucleotide variant (intron variant) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Tremor, hereditary essential, 4 +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Amyotrophic lateral sclerosis type 6 | |
| | | Single nucleotide variant (missense variant +1 more) | FUS-related disorder +3 more | |