KCNJ2

Genes:

• KCNJ16
• KCNJ2

GWAS Disease/Phenotype:

• Primary tooth development (number of teeth)
• Primary tooth development (time to first tooth eruption)

Genes:

• KCNJ2

GWAS Disease/Phenotype:

• Primary tooth development (number of teeth)
• Primary tooth development (time to first tooth eruption)

Genes:

• KCNJ2

GWAS Disease/Phenotype:

• Thyrotoxic hypokalemic periodic paralysis

Genes:

• KCNJ16
• KCNJ2

GWAS Disease/Phenotype:

• Thyrotoxic hypokalemic periodic paralysis

Genes:

• KCNJ2

GWAS Disease/Phenotype:

• QT interval

Genes:

• KCNJ2

GWAS Disease/Phenotype:

• Cardiac repolarization

Genes:

• KCNJ2

GWAS Disease/Phenotype:

• Refractive error

Genes:

• KCNJ2
• SOX9

GWAS Disease/Phenotype:

• Pulmonary function (interaction)

Genes:

• KCNJ2
• SOX9

GWAS Disease/Phenotype:

• Adolescent idiopathic scoliosis (severe)