RS121909379 SLC12A3
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial hypokalemia-hypomagnesemia
Inborn genetic diseases
SLC12A3-related disorder
Renal tubulopathies
Familial hypokalemia-hypomagnesemia
Inborn genetic diseases
SLC12A3-related disorder
Renal tubulopathies
Other Variants in SLC12A3