RS377278120 PCYT2

Health Risk Chr 17:81904928
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Associated Conditions
Spastic paraplegia 82
autosomal recessive
Inborn genetic diseases
Spastic paraplegia 82
autosomal recessive
Inborn genetic diseases
Other Variants in PCYT2
rs778113360 rs1365461027 rs1436764763 rs2510047496 rs751856962 rs953415774 rs763945631 rs2040278710 rs2510045525
Ask Dr. Hemsworth about this variant