| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129934355, LOC129934356 +348 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 | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129934346, LOC129934347 +125 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Deletion | Schizophrenia | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (R10W) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (R10G) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (E26K) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (P29L) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (R32P) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (V49A) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (A72V) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (S114L) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (G126W) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (A128V) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (P133L) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (W135R) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (A142T) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (R183C) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (R188G) | Single nucleotide variant (missense variant) | not specified | |
| | CNNM3, LOC129934366 (R189C) | Single nucleotide variant (missense variant) | not specified | |