RS376679623 DYNC1H1
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Associated Conditions
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Rhizomelic chondrodysplasia punctata type 5
Asphyxiating thoracic dystrophy 3
Charcot-Marie-Tooth disease axonal type 2O
Inborn genetic diseases
Rhizomelic chondrodysplasia punctata type 5
Asphyxiating thoracic dystrophy 3
Other Variants in DYNC1H1