RS587776593 APTX

Health Risk Chr 9:32984711
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What This Variant Does
"CLNSIG=5
Associated Conditions
Ataxia
early-onset
with oculomotor apraxia and hypoalbuminemia
Inborn genetic diseases
Ataxia
early-onset
with oculomotor apraxia and hypoalbuminemia
Inborn genetic diseases
Other Variants in APTX
rs121908131 rs587776594 rs121908132 rs121908133 rs1587330671 rs104894103 rs267606665 rs141493373 rs774597262 rs141195622
Ask Dr. Hemsworth about this variant