RS730882220 FAM20C

Health Risk Chr 7:256001
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Cortical dysplasia
Neonatal death
Severe brain malformation
Abnormal facial shape
Cortical dysplasia
Neonatal death
Severe brain malformation
Abnormal facial shape
Other Variants in FAM20C
rs267606795 rs796051849 rs796051851 rs796051852 rs796051853 rs796051854 rs796051855 rs2115173146 rs796051874 rs797044462
Ask Dr. Hemsworth about this variant