Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11744876
rs11744876
Entrez Id: 1501
Gene Symbol: CTNND2
CTNND2
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014