RS140012781 SLC12A3

Health Risk Chr 16:56886365 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Familial hypokalemia-hypomagnesemia
Bartter syndrome
Inborn genetic diseases
Familial hypokalemia-hypomagnesemia
Bartter syndrome
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
0%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in SLC12A3
rs121909379 rs28936387 rs28936388 rs755560627 rs121909380 rs1347239469 rs121909382 rs121909383 rs2144723103 rs121909384
Ask Dr. Hemsworth about this variant