RS78215018 ASPM
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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