Trait
SNPs associated with Abnormal pupillary function
12 genetic variants across 6 genes have been associated with Abnormal pupillary function in published research. Key genes include FMN2, LINC02354, LOC105375996.
Associated variants12 total
| rsid | Gene | Effect | Evidence |
|---|---|---|---|
| rs186047086 | — | GWAS association (p=5.0e-14) | Major Consortium Study |
| rs540435757 | TNFRSF21 | GWAS association (p=7.0e-14) | Major Consortium Study |
| rs574618841 | — | GWAS association (p=6.0e-13) | Major Consortium Study |
| rs575074431 | — | GWAS association (p=1.0e-12) | Major Consortium Study |
| rs573176829 | — | GWAS association (p=1.0e-12) | Major Consortium Study |
| rs552323668 | NCALD | GWAS association (p=4.0e-12) | Major Consortium Study |
| rs370309668 | — | GWAS association (p=5.0e-12) | Major Consortium Study |
| rs180886267 | FMN2 | GWAS association (p=9.0e-12) | Major Consortium Study |
| rs192917207 | RET | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs536829424 | LINC02354 | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs180958886 | LOC105375996 | GWAS association (p=4.0e-11) | Major Consortium Study |
| rs530546566 | — | GWAS association (p=4.0e-11) | Major Consortium Study |
Associations aggregated from the GWAS Catalog and curated literature. Informational only — not medical advice.