RS200069949 SLC26A1

Health Risk Chr 4:988930
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Associated Conditions
Inborn genetic diseases
Nephrolithiasis susceptibility caused by SLC26A1
Hypersulfaturia
Inborn genetic diseases
Nephrolithiasis susceptibility caused by SLC26A1
Hypersulfaturia
Other Variants in SLC26A1
rs371616275 rs369620087 rs201608921 rs139142520 rs1192140369 rs761530861 rs569131932 rs566030346 rs554618177 rs200471470
Ask Dr. Hemsworth about this variant