RS138977195 SLC12A3
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What This Variant Does
"SLC12A3 gene, c.2221G>
Associated Conditions
Familial hypokalemia-hypomagnesemia
Hypokalemia
Hypermagnesemia
Myalgia
Muscle weakness
Bartter syndrome
SLC12A3-related disorder
Inherited renal tubular disease
Renal tubulopathies
Familial hypokalemia-hypomagnesemia
Hypokalemia
Hypermagnesemia
Myalgia
Muscle weakness
Bartter syndrome
Other Variants in SLC12A3