RS61730252 FAM20C

Health Risk Chr 7:195681
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Associated Conditions
Inborn genetic diseases
FAM20C-related disorder
Inborn genetic diseases
FAM20C-related disorder
Other Variants in FAM20C
rs267606795 rs796051849 rs796051851 rs796051852 rs796051853 rs796051854 rs796051855 rs2115173146 rs796051874 rs797044462
Ask Dr. Hemsworth about this variant