RS140012781 SLC12A3

Health Risk Chr 16:56886366
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial hypokalemia-hypomagnesemia
Bartter syndrome
Inborn genetic diseases
Familial hypokalemia-hypomagnesemia
Bartter syndrome
Inborn genetic diseases
Other Variants in SLC12A3
rs121909379 rs28936387 rs28936388 rs755560627 rs121909380 rs1347239469 rs121909382 rs121909383 rs2144723103 rs121909384
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