rs10811661, None

N. diseases: 22
Disease: Arteriopathic disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arteriopathic disease
CUI: C0852949
Disease: Arteriopathic disease
0.010 GeneticVariation BEFREE The association of rs10811661-T to T2D replicates in our samples, but the variant does not associate with any of the five arterial diseases examined. 18176561 2008