rs61755320, SPG7

N. diseases: 41
Disease: Spastic Paraplegia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Spastic Paraplegia
CUI: C0037772
Disease: Spastic Paraplegia
0.010 GeneticVariation BEFREE SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V. 22571692 2013