RS143232208 FXN

Health Risk Chr 9:69035790
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs143232208, also known as c.11-12 delTC or p.L4RfsX88, is a mutation in the FXN gene on chromosome ...
Associated Conditions
Inborn genetic diseases
Friedreich ataxia 1
Inborn genetic diseases
Friedreich ataxia 1
Other Variants in FXN
rs2133102338 rs1564326640 rs372775073 rs544129099 rs1587832283 rs367974156 rs138034837 rs2539187451 rs2539217018 rs576852565
Ask Dr. Hemsworth about this variant