RS1064793391 SUMF1

Health Risk Chr 3:4417183
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Multiple sulfatase deficiency
Inborn genetic diseases
Multiple sulfatase deficiency
Other Variants in SUMF1
rs775324176 rs137852844 rs137852845 rs137852846 rs137852847 rs137852848 rs137852849 rs2124822282 rs770241913 rs137852850
Ask Dr. Hemsworth about this variant