rs17215437, KCNE3

N. diseases: 4
Disease: Familial Periodic Paralysis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial Periodic Paralysis
CUI: C0030443
Disease: Familial Periodic Paralysis
0.020 GeneticVariation BEFREE Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation. 15037716 2004
Familial Periodic Paralysis
CUI: C0030443
Disease: Familial Periodic Paralysis
0.020 GeneticVariation BEFREE These observations weaken the proposal that MiRP2-R83H causes periodic paralysis. 14504341 2003