RS119476050 ATL1

Health Risk Chr 14:50628154
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary spastic paraplegia 3A
Inborn genetic diseases
Hereditary spastic paraplegia 3A
Inborn genetic diseases
Other Variants in ATL1
rs119476046 rs119476047 rs119476048 rs119476049 rs28939094 rs119476051 rs1595625206 rs863223314 rs137852657 rs1555365597
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