Gene: KCNJ18 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs527236158
rs527236158
KCNJ18
0.800 GeneticVariation UNIPROT A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. 27178871

2016
dbSNP: rs527236159
rs527236159
KCNJ18
0.800 GeneticVariation UNIPROT A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. 27178871

2016
dbSNP: rs672601244
rs672601244
KCNJ18
0.800 GeneticVariation UNIPROT A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. 27178871

2016
dbSNP: rs527236158
rs527236158
KCNJ18
0.800 GeneticVariation UNIPROT The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. 25885757

2015
dbSNP: rs527236159
rs527236159
KCNJ18
0.800 GeneticVariation UNIPROT The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. 25885757

2015
dbSNP: rs672601244
rs672601244
KCNJ18
0.800 GeneticVariation UNIPROT The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. 25885757

2015
dbSNP: rs527236158
rs527236158
KCNJ18
0.800 GeneticVariation UNIPROT Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. 21665951

2011
dbSNP: rs527236159
rs527236159
KCNJ18
0.800 GeneticVariation UNIPROT Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. 21665951

2011
dbSNP: rs672601244
rs672601244
KCNJ18
0.800 GeneticVariation UNIPROT Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. 21665951

2011
dbSNP: rs527236158
rs527236158
KCNJ18
0.800 GeneticVariation UNIPROT Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. 20074522

2010
dbSNP: rs527236159
rs527236159
KCNJ18
0.800 GeneticVariation UNIPROT Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. 20074522

2010
dbSNP: rs672601244
rs672601244
KCNJ18
0.800 GeneticVariation UNIPROT Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. 20074522

2010
dbSNP: rs527236152
rs527236152
KCNJ18
0.700 GeneticVariation UNIPROT A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. 27178871

2016
dbSNP: rs527236154
rs527236154
KCNJ18
0.700 GeneticVariation UNIPROT A novel Kir2.6 mutation associated with hypokalemic periodic paralysis. 27178871

2016
dbSNP: rs527236152
rs527236152
KCNJ18
0.700 GeneticVariation UNIPROT The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. 25885757

2015
dbSNP: rs527236154
rs527236154
KCNJ18
0.700 GeneticVariation UNIPROT The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. 25885757

2015
dbSNP: rs527236152
rs527236152
KCNJ18
0.700 GeneticVariation UNIPROT Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. 21665951

2011
dbSNP: rs527236154
rs527236154
KCNJ18
0.700 GeneticVariation UNIPROT Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. 21665951

2011
dbSNP: rs527236152
rs527236152
KCNJ18
0.700 GeneticVariation UNIPROT Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. 20074522

2010
dbSNP: rs527236154
rs527236154
KCNJ18
0.700 GeneticVariation UNIPROT Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. 20074522

2010