rs368453549, BRD4

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
0.010 GeneticVariation BEFREE We have identified DCTN1 p.K56R in patients with PSP. 27132499 2016