rs2896905, SLC2A13

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Caffeine related disorders
CUI: C0236734
Disease: Caffeine related disorders
0.010 GeneticVariation BEFREE However, with a combined smoking and caffeine intake exposure, we found a significant interaction with rs2896905 at SLC2A13, near LRRK2 (p uncorrected = 0.0008). 22763023 2012