rs104893877, SNCA

N. diseases: 59
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Memory impairment
CUI: C0233794
Disease: Memory impairment
0.020 GeneticVariation BEFREE Our results directly implicate tau as a mediator of specific human mutant A53T αS-mediated abnormalities related to deficits in hippocampal neurotransmission and suggest a mechanism for memory impairment that occurs as a consequence of synaptic dysfunction rather than synaptic or neuronal loss. 31168644 2019
Memory impairment
CUI: C0233794
Disease: Memory impairment
0.020 GeneticVariation BEFREE A53T mice also exhibit spatial memory deficits at 6 and 12 months, as demonstrated by Y-maze performance. 23936403 2013