RS587778791 KIF1A

Health Risk Chr 2:240757337
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neuropathy
hereditary sensory
type 2C
hereditary sensory and autonomic
type 2A
Hereditary spastic paraplegia 30
Intellectual disability
autosomal dominant 9
KIF1A-related disorder
Neuropathy
hereditary sensory
type 2C
hereditary sensory and autonomic
type 2A
Hereditary spastic paraplegia 30
Other Variants in KIF1A
rs387906798 rs387906799 rs387907259 rs587778798 rs116297894 rs190997558 rs371737085 rs672601370 rs672601369 rs672601371
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