rs63750399(A;T)
From SNPedia
| Mutation considered pathogenic for Alzheimer disease |
| Is a | genotype |
| of | rs63750399 |
| Gene | APP |
| Chromosome | 21 |
| Position | 25,891,787 |
| mentioned | by |
| Magnitude | 7 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 7 | Mutation considered pathogenic for Alzheimer disease |
| (A;T) | 7 | Mutation considered pathogenic for Alzheimer disease |
see discussion at rs63750399
