RS1057520304 SLC12A1

Health Risk Chr 15:48251657
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What This Variant Does
"CLNSIG=5
Associated Conditions
Bartter disease type 1
Inborn genetic diseases
Bartter disease type 1
Inborn genetic diseases
Other Variants in SLC12A1
rs137853158 rs137853159 rs774515747 rs1057519608 rs200417237 rs765347751 rs886039870 rs779588655 rs142646329 rs747229048
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