Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1186689
rs1186689
Entrez Id: 3765;3766
Gene Symbol: KCNJ9;KCNJ10
KCNJ9;KCNJ10
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE These results demonstrated that KCNJ10 (rs1186689) polymorphisms was correlated with ASD susceptibility in Chinese Han children, and the abnormal expression of Kir2.1 and Kir4.1 in ASD model rats suggested a mechanism by which Kir channels may play a role in ASD. 30304693 2018
dbSNP: rs1186688
rs1186688
Entrez Id: 3765;3766
Gene Symbol: KCNJ9;KCNJ10
KCNJ9;KCNJ10
CUI: C0038644
Disease:
Sudden infant death syndrome
0.010 GeneticVariation BEFREE The CC genotype of rs72878794 in the AQP4 gene and a combination of the CC genotype in rs17375748, rs1130183, rs12133079 and rs1186688 in KCNJ10 (4xCC) were found to be associated with SIDS. 28520217 2017
dbSNP: rs2737703
rs2737703
Entrez Id: 3765
Gene Symbol: KCNJ9
KCNJ9
CUI: C0027498
Disease:
Nausea and vomiting
0.010 GeneticVariation BEFREE No significant association with severity of phenotype versus genotype of the 11 SNPs was observed except for unadjusted data for rs2737703.There was no significant difference between severity or incidence of IVPCA morphine-induced nausea and vomiting and genotype (11 SNPs). 28640078 2017
dbSNP: rs61822012
rs61822012
Entrez Id: 3765;3766
Gene Symbol: KCNJ9;KCNJ10
KCNJ9;KCNJ10
CUI: C0014544
Disease:
Epilepsy
0.010 GeneticVariation BEFREE However, no statistically significant association was found between rs61822012 polymorphism and epilepsy. 25008907 2015