RS773251870 ITPR1

Health Risk Chr 3:4684296
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Associated Conditions
Autosomal dominant cerebellar ataxia
Inborn genetic diseases
Autosomal dominant cerebellar ataxia
Inborn genetic diseases
Other Variants in ITPR1
rs121912425 rs397514535 rs397514536 rs61757111 rs371988852 rs797044955 rs863224882 rs869312685 rs878853171 rs878853172
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