RS145854903 FXN

Health Risk Chr 9:69035900
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What This Variant Does
"rs145854903, also known as c.118 C&gt
Associated Conditions
Hypertrophic cardiomyopathy
Inborn genetic diseases
Friedreich ataxia 1
Hypertrophic cardiomyopathy
Inborn genetic diseases
Friedreich ataxia 1
Other Variants in FXN
rs2133102338 rs1564326640 rs372775073 rs544129099 rs1587832283 rs367974156 rs138034837 rs2539187451 rs2539217018 rs576852565
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