RS797045164 KIF1A

Health Risk Chr 2:240785063
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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
Syndromic intellectual disability
Inborn genetic diseases
Spastic paraplegia 30A
autosomal dominant
Intellectual disability
autosomal dominant 9
PEHO syndrome
Hereditary spastic paraplegia 30
Other Variants in KIF1A
rs387906798 rs387906799 rs387907259 rs587778791 rs587778798 rs116297894 rs190997558 rs371737085 rs672601370 rs672601369
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