Hereditary Motor and Sensory Neuropathy with Optic Atrophy
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Associated Variants (30)
| RSID | Gene | Evidence |
|---|---|---|
| RS144860227 | MFN2 | strong |
| RS2138792385 | MTRFR | strong |
| RS200441797 | MFN2 | strong |
| RS1639390139 | MFN2 | strong |
| RS1040702840 | MFN2 | strong |
| RS1553145402 | MFN2 | strong |
| RS148441213 | MFN2 | strong |
| RS1057517987 | MFN2 | strong |
| RS571011689 | MFN2 | strong |
| RS145994616 | MFN2 | strong |
| RS141974160 | MFN2 | strong |
| RS138345244 | MFN2 | strong |
| RS141468012 | MFN2 | strong |
| RS864622480 | MFN2 | strong |
| RS863224967 | MFN2 | strong |
| RS28940292 | MFN2 | strong |
| RS369762154 | MFN2 | strong |
| RS863224066 | MFN2 | strong |
| RS147136530 | MFN2 | strong |
| RS201715603 | MFN2 | strong |
| RS137960129 | MFN2 | strong |
| RS387906991 | MFN2 | strong |
| RS138382758 | MFN2 | strong |
| RS119103268 | MFN2 | strong |
| RS119103267 | MFN2 | strong |
| RS119103266 | MFN2 | strong |
| RS119103265 | MFN2 | strong |
| RS119103264 | MFN2 | strong |
| RS119103263 | MFN2 | strong |
| RS28940296 | MFN2 | strong |