RS773138218 VRK1

Health Risk Chr 14:96846144
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pontocerebellar hypoplasia type 1A
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal recessive 10
Pontocerebellar hypoplasia type 1A
Inborn genetic diseases
Neuronopathy
distal hereditary motor
autosomal recessive 10
Other Variants in VRK1
rs137853063 rs387906830 rs139476915 rs794727029 rs371295780 rs772731615 rs771364038 rs61736727 rs541660707 rs767585930
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