RS144336311 SNX27

Health Risk Chr 1:151683443
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Associated Conditions
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Other Variants in SNX27
rs1670312400 rs2525156811 rs2525037609 rs1571881557 rs574654968 rs1346732190 rs2102724265 rs2102676931 rs2102690228 rs1553266166
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