RS397514535 ITPR1

Health Risk Chr 3:4706193
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spinocerebellar ataxia type 29
Inborn genetic diseases
Neurodevelopmental disorder
Spinocerebellar ataxia type 15/16
Gillespie syndrome
Spinocerebellar ataxia type 29
Inborn genetic diseases
Neurodevelopmental disorder
Spinocerebellar ataxia type 15/16
Gillespie syndrome
Other Variants in ITPR1
rs121912425 rs397514536 rs61757111 rs371988852 rs797044955 rs863224882 rs869312685 rs878853171 rs878853172 rs878853173
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