rs121917767, UCHL1

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
0.010 GeneticVariation BEFREE We examined the association of HD with the I93M mutation and S18Y polymorphism in 138 HD patients and 136 control subjects, but we did not identify the I93M mutation. 12123845 2002