RS886041126 AP4M1

Health Risk Chr 7:100106841
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 50
Spastic paraplegia
Hereditary spastic paraplegia 50
Spastic paraplegia
Other Variants in AP4M1
rs387906838 rs730882249 rs146262009 rs797045249 rs367614875 rs138437966 rs754498075 rs372787797 rs147738731 rs141754568
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