RS672601362 KIF1A
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What This Variant Does
"CLNSIG=4
Associated Conditions
Intellectual disability
autosomal dominant 9
Hereditary spastic paraplegia 30
Inborn genetic diseases
Neuropathy
hereditary sensory
type 2C
Neurodevelopmental delay
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
Intellectual disability
autosomal dominant 9
Intellectual disability
Other Variants in KIF1A