rs1006737, CACNA1C

N. diseases: 27
Disease: Impaired cognition ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
0.010 GeneticVariation BEFREE Our results do not support that the common genetic risk variants in rs6265 and rs1006737 are associated with cognitive dysfunction. 27221213 2016