RS786204767 CPT1C

Health Risk Chr 19:49692361
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 73
Hereditary spastic paraplegia 73
Other Variants in CPT1C
rs2514088767 rs566644989 rs762616491 rs1019515406 rs141453772 rs759904221 rs2514147270 rs767517922 rs1447368316 rs748659009
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