RS1420939606 VRK1
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Associated Conditions
Inborn genetic diseases
Pontocerebellar hypoplasia type 1A
Neuronopathy
distal hereditary motor
autosomal recessive 10
Inborn genetic diseases
Pontocerebellar hypoplasia type 1A
Neuronopathy
distal hereditary motor
autosomal recessive 10
Other Variants in VRK1