RS1064794935 KIF1A

Health Risk Chr 2:240797716
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
Intellectual disability
autosomal dominant 9
See cases
KIF1A related neurological disorder
Inborn genetic diseases
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
Intellectual disability
autosomal dominant 9
Other Variants in KIF1A
rs387906798 rs387906799 rs387907259 rs587778791 rs587778798 rs116297894 rs190997558 rs371737085 rs672601370 rs672601369
Ask Dr. Hemsworth about this variant