RS672601369 KIF1A

Health Risk Chr 2:240783780
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 9
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
KIF1A-related disorder
Intellectual disability
autosomal dominant 9
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
KIF1A-related disorder
Other Variants in KIF1A
rs387906798 rs387906799 rs387907259 rs587778791 rs587778798 rs116297894 rs190997558 rs371737085 rs672601370 rs672601371
Ask Dr. Hemsworth about this variant