RS768449676 RTN2

Health Risk Chr 19:45493254
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 12
Spastic paraplegia
Hereditary spastic paraplegia 12
Spastic paraplegia
Other Variants in RTN2
rs763387041 rs145653668 rs761286207 rs748397131 rs1568625691 rs1568624823 rs201387324 rs745409162 rs201863499 rs748824542
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