rs63750306, PSEN1

N. diseases: 17
Disease: Cerebellar atrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cerebellar atrophy
CUI: C0740279
Disease: Cerebellar atrophy
0.010 GeneticVariation BEFREE The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family. 28532646 2017