Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17215437
rs17215437
KCNE3
0.020 GeneticVariation BEFREE Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation. 15037716

2004
dbSNP: rs17215437
rs17215437
KCNE3
0.020 GeneticVariation BEFREE These observations weaken the proposal that MiRP2-R83H causes periodic paralysis. 14504341

2003