Gene: C9orf72 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.030 GeneticVariation phenotype BEFREE C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism. 28124431 2017
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.030 Biomarker phenotype BEFREE C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland China. 26810537 2016
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.030 Biomarker phenotype BEFREE Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. 22650353 2013