Gene: C9orf72 ×
Source: GWASDB ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.800 GeneticVariation disease GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638 2013
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.800 GeneticVariation disease GWASDB Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728 2013
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.800 GeneticVariation disease GWASDB Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. 20801717 2010
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.800 GeneticVariation disease GWASDB Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. 20801718 2010
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72 		0.800 GeneticVariation disease GWASDB Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. 19734901 2009