rs1311839715, KCNJ18

N. diseases: 3
Disease: Hyperthyroidism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperthyroidism
CUI: C0020550
Disease: Hyperthyroidism
0.010 GeneticVariation BEFREE A novel KCNJ18 mutation, G169R, was first reported to be associated with hypokalemic periodic paralysis without hyperthyroidism. 27178871 2016