RS587783239 ASPM

Health Risk Chr 1:197121931
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 5
primary
autosomal recessive
Inborn genetic diseases
Microcephaly 5
primary
autosomal recessive
Inborn genetic diseases
Other Variants in ASPM
rs199422135 rs189678019 rs199422184 rs137852994 rs137852995 rs137852996 rs137852997 rs199422163 rs145489194 rs199422138
Ask Dr. Hemsworth about this variant