RS532290202 SLC12A2

Health Risk Chr 5:128167859
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SLC12A2
rs886040968 rs1581138934 rs1581138944 rs1581138932 rs1581138965 rs1762258987 rs1762648450 rs1763563407 rs1761279419 rs1763249655
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