RS119476046 ATL1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary spastic paraplegia 3A
Neuropathy
hereditary sensory
type 1D
Spastic paraplegia
Hereditary spastic paraplegia
Hereditary spastic paraplegia 3A
Neuropathy
hereditary sensory
type 1D
Spastic paraplegia
Hereditary spastic paraplegia
Population Frequencies
gnomAD ALL
0%
Other Variants in ATL1