RS201915239 RNF168

Health Risk Chr 3:196487566
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
RIDDLE syndrome
RNF168-related disorder
RIDDLE syndrome
RNF168-related disorder
Other Variants in RNF168
rs1577516447 rs1047608955 rs148275050 rs755314562 rs2108657396 rs149298083 rs2108657437 rs375915880 rs2108644029 rs371453745
Ask Dr. Hemsworth about this variant