RS879253888 KIF1A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Intellectual disability
autosomal dominant 9
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
hereditary sensory and autonomic
type 2A
KIF1A-related disorder
Neuropathy
hereditary sensory
type 2C
Intellectual disability
autosomal dominant 9
Other Variants in KIF1A