RS201713384 CNOT1

Health Risk Chr 16:58580648
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Associated Conditions
Inborn genetic diseases
Holoprosencephaly 12 with or without pancreatic agenesis
Inborn genetic diseases
Holoprosencephaly 12 with or without pancreatic agenesis
Other Variants in CNOT1
rs1567417422 rs1597562609 rs2042382430 rs2040599000 rs1567396193 rs2040286240 rs2042382246 rs2151940462 rs2151904583 rs2151980137
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