RS104894103 APTX

Health Risk Chr 9:32974495
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What This Variant Does
"[OMIM:?]
Associated Conditions
Ataxia
early-onset
with oculomotor apraxia and hypoalbuminemia
Inborn genetic diseases
APTX-related disorder
Hereditary ataxia
Ataxia
early-onset
with oculomotor apraxia and hypoalbuminemia
Inborn genetic diseases
APTX-related disorder
Hereditary ataxia
Other Variants in APTX
rs587776593 rs121908131 rs587776594 rs121908132 rs121908133 rs1587330671 rs267606665 rs141493373 rs774597262 rs141195622
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