Disease: periodic paralysis (finding) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17215437
rs17215437
Entrez Id: 10008
Gene Symbol: KCNE3
KCNE3
CUI: C1279412
Disease:
periodic paralysis (finding) 		0.020 GeneticVariation BEFREE Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation. 15037716 2004
dbSNP: rs17215437
rs17215437
Entrez Id: 10008
Gene Symbol: KCNE3
KCNE3
CUI: C1279412
Disease:
periodic paralysis (finding) 		0.020 GeneticVariation BEFREE These observations weaken the proposal that MiRP2-R83H causes periodic paralysis. 14504341 2003