RS78215018 ASPM

Health Risk Chr 1:197101581
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Associated Conditions
Microcephaly 5
primary
autosomal recessive
Inborn genetic diseases
Intellectual disability
ASPM-related disorder
Microcephaly 5
primary
autosomal recessive
Inborn genetic diseases
Intellectual disability
ASPM-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
CFHR2 protein levels C OR: 0.44 3E-31 PubMed
Other Variants in ASPM
rs199422135 rs189678019 rs199422184 rs137852994 rs137852995 rs137852996 rs137852997 rs199422163 rs145489194 rs199422138
Ask Dr. Hemsworth about this variant