RS1060503526 PKD2

Health Risk Chr 4:88038380
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant polycystic kidney disease
Polycystic kidney disease 2
Inborn genetic diseases
Autosomal dominant polycystic kidney disease
Polycystic kidney disease 2
Inborn genetic diseases
Other Variants in PKD2
rs121918039 rs121918040 rs121918041 rs1560598042 rs121918042 rs757757289 rs121918043 rs1560621750 rs398122932 rs398123306
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