| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | BACE1, LOC126861353 (M331V +6 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BACE1, BACE1-AS (R271C +6 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BACE1, LOC126861353 (T312I +6 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BACE1, LOC126861353 (D382E +6 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BACE1, LOC126861353 (R362C +6 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BACE1, LOC126861353 (T410N +6 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BACE1, LOC130006821 (G33C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene