rs1051266, SLC19A1

N. diseases: 41
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
0.010 GeneticVariation BEFREE No direct association was found between variant (G) allele or genotype of rs1051266 with AD and VaD cases. 24554143 2014