RS2234675 PAX3
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Associated Conditions
Congenital diaphragmatic hernia
Waardenburg syndrome
Craniofacial-deafness-hand syndrome
Waardenburg syndrome type 1
Congenital diaphragmatic hernia
Waardenburg syndrome
Craniofacial-deafness-hand syndrome
Waardenburg syndrome type 1
GWAS Studies (5)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| T2 brain MRIs Unsupervised Deep learning derived Imaging Phenotypes (dimension 119) | — | — | 5E-11 | PubMed |
| Brain morphology (MOSTest) | — | — | 7E-11 | PubMed |
| aseg lh volume Cerebellum-Cortex | T | OR: 0.15 | 2E-10 | PubMed |
| Brain region volumes | — | — | 1E-9 | PubMed |
| aseg rh volume Cerebellum-Cortex | T | OR: 0.14 | 1E-8 | PubMed |
Other Variants in PAX3