RS140299648 SLC26A1

Health Risk Chr 4:989935
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Associated Conditions
Inborn genetic diseases
Hypersulfaturia
Nephrolithiasis susceptibility caused by SLC26A1
Inborn genetic diseases
Hypersulfaturia
Nephrolithiasis susceptibility caused by SLC26A1
Other Variants in SLC26A1
rs200069949 rs201608921 rs139142520 rs1192140369 rs761530861 rs371616275 rs569131932 rs566030346 rs554618177 rs369620087
Ask Dr. Hemsworth about this variant