RS2525037609 SNX27

Health Risk Chr 1:151668558
Upload your DNA to see your genotype for this variant.
Associated Conditions
Severe myoclonic epilepsy in infancy
Severe myoclonic epilepsy in infancy
Other Variants in SNX27
rs2102681464 rs2525156811 rs1571881557 rs574654968 rs1346732190 rs2102724265 rs2102676931 rs2102690228 rs1670312400 rs1553266166
Ask Dr. Hemsworth about this variant