rs148398509, HCN4

N. diseases: 5
Disease: Tic disorder ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Tic disorder
CUI: C0040188
Disease: Tic disorder
0.010 GeneticVariation BEFREE Together with the common KCNE1 variant S38G, previously proposed as a genetic modifier of AF, HCN4-P883R may provide a substrate for the development of AF and TIC. 31481236 2019