| | ADAMTS19, ADAMTS19-AS1 +688 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | ADAMTS19, ADAMTS19-AS1 +377 more | Copy number loss | See cases | |
| | LOC129994580, LOC129994581 +336 more | Copy number loss | See cases | |
| | ACSL6, ACSL6-AS1 +200 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Microsatellite | not provided | |
| | LOC129994526, SLC12A2 (E2Q) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (G14V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | |
| | LOC129994526, SLC12A2 (V18F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Deletion (inframe_deletion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (P43A) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A46V) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A49P) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (D52E) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (E59D) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (G60V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC129994526, SLC12A2 (A62T) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A64T) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (D66N) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC129994526, SLC12A2 (G67E) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (R70G) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (P71S) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | SLC12A2, LOC129994526 (L72M) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (L72W) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC129994526, SLC12A2 (P76R) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (S79R) | Single nucleotide variant (missense variant +1 more) | Hearing loss, autosomal dominant 78 +3 more | |
| | LOC129994526, SLC12A2 (F81L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | |
| | LOC129994526, SLC12A2 (A90P) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A93S) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | SLC12A2-related condition +1 more | |
| | | Duplication (inframe_insertion +1 more) | not provided | |
| | | Deletion (inframe_deletion +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Duplication (inframe_insertion +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided +1 more | |
| | | Microsatellite (inframe_insertion +1 more) | Kilquist syndrome +3 more | |
| | | Microsatellite (inframe_insertion +1 more) | Kilquist syndrome +3 more | |
| | | Microsatellite (inframe_deletion +1 more) | not provided | |
| | | Microsatellite (inframe_deletion +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A107del) | Microsatellite (inframe_deletion +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (non-coding transcript variant +1 more) | Inborn genetic diseases +1 more | |
| | | Deletion (inframe_deletion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A97T) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (inframe_deletion +1 more) | not provided | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Deletion (inframe_deletion +1 more) | not provided | |
| | | Duplication (inframe_insertion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Deletion (inframe_deletion +1 more) | not provided | |
| | | Duplication (inframe_insertion +1 more) | not provided | |
| | | Deletion (inframe_deletion +1 more) | SLC12A2-related condition +1 more | |
| | | Duplication (inframe_insertion +1 more) | not provided | |
| | LOC129994526, SLC12A2 (A101V) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Duplication (non-coding transcript variant +1 more) | not provided | |
| | | Deletion (inframe_deletion +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |