RS267606717 CEP152

Health Risk Chr 15:48793359
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What This Variant Does
"CLNSIG=255
Associated Conditions
Microcephaly 9
primary
autosomal recessive
CEP152-related disorder
Seckel syndrome 5
Microcephaly 9
primary
autosomal recessive
CEP152-related disorder
Seckel syndrome 5
Other Variants in CEP152
rs267606718 rs966888627 rs1349385657 rs201342438 rs1048042 rs77745570 rs149478199 rs587783424 rs138151279 rs74553953
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