rs6798742, ATXN7

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Spinocerebellar Ataxia Type 7
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
0.010 GeneticVariation BEFREE A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population. 28597910 2017