RS182018947 CEP152

Health Risk Chr 15:48767448
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 9
primary
autosomal recessive
Seckel syndrome 5
Inborn genetic diseases
CEP152-related disorder
Microcephaly 9
primary
autosomal recessive
Seckel syndrome 5
Inborn genetic diseases
CEP152-related disorder
Other Variants in CEP152
rs267606717 rs267606718 rs966888627 rs1349385657 rs201342438 rs1048042 rs77745570 rs149478199 rs587783424 rs138151279
Ask Dr. Hemsworth about this variant