RS747831095 CDK5RAP2

Health Risk Chr 9:120443671
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 3
primary
autosomal recessive
Inborn genetic diseases
Microcephaly 3
primary
autosomal recessive
Inborn genetic diseases
Other Variants in CDK5RAP2
rs199422126 rs387906274 rs398122971 rs374351172 rs373278668 rs587783393 rs145165171 rs587783396 rs587783392 rs141004029
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