Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11637611
rs11637611
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. 22833209

2011