RS397514619 ATP2B3

Health Risk Chr X:153565081
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What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked progressive cerebellar ataxia
Inborn genetic diseases
X-linked progressive cerebellar ataxia
Inborn genetic diseases
Other Variants in ATP2B3
rs724160009 rs724160011 rs724160012 rs368215361 rs782596945 rs781901998 rs149114271 rs1603040061 rs782756404 rs2124491843
Ask Dr. Hemsworth about this variant