RS515726137 ATP8B1

Health Risk Chr 18:57669422
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive familial intrahepatic cholestasis type 1
Inborn genetic diseases
Progressive familial intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis type 1
Progressive familial intrahepatic cholestasis type 1
Inborn genetic diseases
Progressive familial intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis type 1
Other Variants in ATP8B1
rs111033609 rs121909098 rs121909099 rs387906381 rs121909100 rs2122653939 rs121909101 rs1057523495 rs34719006 rs121909103
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