RS869312944 PKD1

Health Risk Chr 16:2100398
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Autosomal dominant polycystic kidney disease
Polycystic kidney disease
adult type
Inborn genetic diseases
Autosomal dominant polycystic kidney disease
Polycystic kidney disease
adult type
Other Variants in PKD1
rs2151684070 rs199476094 rs1567154953 rs199476095 rs199476096 rs199476097 rs199476098 rs1218054241 rs1567192790 rs1567204631
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