rs17215437, KCNE3

N. diseases: 4
Disease: periodic paralysis (finding) ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
periodic paralysis (finding)
CUI: C1279412
Disease: periodic paralysis (finding)
0.020 GeneticVariation BEFREE Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation. 15037716 2004
periodic paralysis (finding)
CUI: C1279412
Disease: periodic paralysis (finding)
0.020 GeneticVariation BEFREE These observations weaken the proposal that MiRP2-R83H causes periodic paralysis. 14504341 2003