RS886039392 ITPR1

Health Risk Chr 3:4645678
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 15/16
Gillespie syndrome
Neurodevelopmental disorder
Inborn genetic diseases
Spinocerebellar ataxia type 29
Spinocerebellar ataxia type 15/16
Gillespie syndrome
Neurodevelopmental disorder
Other Variants in ITPR1
rs121912425 rs397514535 rs397514536 rs61757111 rs371988852 rs797044955 rs863224882 rs869312685 rs878853171 rs878853172
Ask Dr. Hemsworth about this variant