RS149176738 CEP152

Health Risk Chr 15:48767078
Upload your DNA to see your genotype for this variant.
Associated Conditions
Seckel syndrome 5
Microcephaly 9
primary
autosomal recessive
Seckel syndrome 5
Microcephaly 9
primary
autosomal recessive
Other Variants in CEP152
rs267606717 rs267606718 rs966888627 rs1349385657 rs201342438 rs1048042 rs77745570 rs149478199 rs587783424 rs138151279
Ask Dr. Hemsworth about this variant