| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129932646, LOC129932647 +967 more | Copy number gain | See cases | |
| | LOC129932948, LOC129932949 +954 more | Copy number gain | See cases | |
| | LOC129932666, LOC129932667 +954 more | Copy number gain | See cases | |
| | LOC128772241, LOC128772242 +952 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129932613, LOC129932614 +949 more | Copy number gain | See cases | |
| | LOC129932859, LOC129932860 +869 more | Copy number gain | See cases | |
| | LOC129932775, LOC129932776 +655 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 | |
| | LOC129932908, LOC129932909 +270 more | Copy number loss | Intellectual disability, autosomal dominant 22 | |
| | LOC110121264, LOC110121265 +301 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 | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | SNORA100, SPMIP3 +274 more | Copy number loss | Intellectual disability, autosomal dominant 22 | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129932958, LOC129932959 +253 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 | |
| | | Copy number loss | Intellectual disability, autosomal dominant 22 | |
| | | Copy number loss | See cases | |
| | LOC122152353, PLD5 +15 more | Deletion | Senior-Loken syndrome 7 +1 more | |
| | | Copy number loss | See cases | |
| | | Copy number loss | Intellectual disability, autosomal dominant 22 | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC112577566, LOC122152351 +27 more | Copy number loss | See cases | |
| | LINC01743, LINC02774 +235 more | Copy number loss | Intellectual disability, autosomal dominant 22 | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | AKT3, LOC110120698 +7 more | Copy number loss | See cases | |
| | AKT3, LOC122152351 +6 more | Copy number loss | See cases | |
| | AKT3, LOC122152351 +5 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | AKT3, LOC110120698 +4 more | Copy number loss | See cases | |
| | AKT3, LOC110120698 +4 more | Copy number loss | See cases | |
| | | Single nucleotide variant (intron variant) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (intron variant) | Bardet-Biedl syndrome 16 +1 more | |
| | | Single nucleotide variant (intron variant) | Bardet-Biedl syndrome 16 +1 more | |
| | | Single nucleotide variant (intron variant) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +2 more | |
| | | Duplication (inframe_insertion +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (A706V +3 more) | Single nucleotide variant (missense variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (Q375E +3 more) | Single nucleotide variant (missense variant +1 more) | Bardet-Biedl syndrome 16 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | SDCCAG8-related disorder +2 more | |
| | AKT3, SDCCAG8 (L379V +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | AKT3, SDCCAG8 (N587Y +3 more) | Single nucleotide variant (missense variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Bardet-Biedl syndrome 16 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | GConflicting classifications of pathogenicity |
| | AKT3, SDCCAG8 (R390fs +3 more) | Microsatellite (frameshift variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | Bardet-Biedl syndrome 16 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Bardet-Biedl syndrome 16 +1 more | |
| | AKT3, SDCCAG8 (S392N +3 more) | Single nucleotide variant (missense variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (E599D +3 more) | Single nucleotide variant (missense variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (R399W +3 more) | Single nucleotide variant (missense variant +1 more) | Bardet-Biedl syndrome 16 +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | SDCCAG8-related disorder | |
| | AKT3, SDCCAG8 (R401W +3 more) | Single nucleotide variant (missense variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (R734Q +3 more) | Single nucleotide variant (missense variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (T703I +3 more) | Single nucleotide variant (missense variant +1 more) | SDCCAG8-related disorder +2 more | |
| | | Single nucleotide variant (splice donor variant +1 more) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (intron variant) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (intron variant) | Senior-Loken syndrome 7 +1 more | |
| | | Single nucleotide variant (intron variant) | Bardet-Biedl syndrome 16 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Senior-Loken syndrome 7 +1 more | |
| | | Duplication (synonymous variant +2 more) | Bardet-Biedl syndrome 16 +1 more | |
| | | Deletion (frameshift variant +2 more) | SDCCAG8-related disorder +2 more | |
| | | Single nucleotide variant (missense variant +2 more) | Senior-Loken syndrome 7 +1 more | |
| | AKT3, SDCCAG8 (M610V +4 more) | Single nucleotide variant (missense variant +1 more) | Bardet-Biedl syndrome 16 +1 more | |
| | AKT3, SDCCAG8 (M407I +3 more) | Single nucleotide variant (synonymous variant +2 more) | Senior-Loken syndrome 7 +1 more | |