RS141935559 FXN

Health Risk Chr 9:69035936
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What This Variant Does
"rs141935559, also known as c.157 insC or p.R53PfsX40, is a mutation in the FXN gene on chromosome 9....
Associated Conditions
Friedreich ataxia
Friedreich ataxia
Other Variants in FXN
rs2133102338 rs1564326640 rs372775073 rs544129099 rs1587832283 rs367974156 rs138034837 rs2539187451 rs2539217018 rs576852565
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