Show All Literature Evidence.

Query Genotype: 2 A2M
Query Phenotype: HP:0002185 Neurofibrillary tangles


Literature Evidence

2 A2M HP:0002185 Neurofibrillary tangles point mutations Association 24011543 The SNP rs669 has been associated with argyrophilic grain disease, a disease that may have neurofibrillary lesions that are typical of AD, but meta-analyses of rs3832852 and rs669 association studies show no significant allele frequency differences between AD cases and controls, even after stratification by APOE epsilon4.