RS387906941 ATL1

Health Risk Chr 14:50628157
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 3A
Hereditary spastic paraplegia
Inborn genetic diseases
Neuropathy
hereditary sensory
type 1D
Hereditary spastic paraplegia 3A
Hereditary spastic paraplegia
Inborn genetic diseases
Neuropathy
hereditary sensory
type 1D
Other Variants in ATL1
rs119476046 rs119476047 rs119476048 rs119476049 rs28939094 rs119476050 rs119476051 rs1595625206 rs863223314 rs137852657
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