RS763622631 FAM20C

Health Risk Chr 7:195556
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Associated Conditions
Inborn genetic diseases
Lethal osteosclerotic bone dysplasia
Inborn genetic diseases
Lethal osteosclerotic bone dysplasia
Other Variants in FAM20C
rs267606795 rs796051849 rs796051851 rs796051852 rs796051853 rs796051854 rs796051855 rs2115173146 rs796051874 rs797044462
Ask Dr. Hemsworth about this variant