RS387906799 KIF1A

Health Risk Chr 2:240788118
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 9
PEHO syndrome
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
KIF1A-related disorder
Intellectual disability
autosomal dominant 9
PEHO syndrome
Hereditary spastic paraplegia 30
Neuropathy
hereditary sensory
type 2C
Other Variants in KIF1A
rs387906798 rs387907259 rs587778791 rs587778798 rs116297894 rs190997558 rs371737085 rs672601370 rs672601369 rs672601371
Ask Dr. Hemsworth about this variant