Trait
SNPs associated with Device Complication
12 genetic variants across 6 genes have been associated with Device Complication in published research. Key genes include APOL1, EPHB1, GFRA2.
Associated variants12 total
| rsid | Gene | Effect | Evidence |
|---|---|---|---|
| rs4977575 | — | GWAS association (p=9.0e-20) | Major Consortium Study |
| rs55730499 | LPA | GWAS association (p=3.0e-19) | Major Consortium Study |
| rs7859727 | — | GWAS association (p=2.0e-17) | Major Consortium Study |
| rs9622363 | APOL1 | GWAS association (p=1.0e-13) | Major Consortium Study |
| rs190633440 | — | GWAS association (p=3.0e-13) | Major Consortium Study |
| rs535426653 | KCNN2 | GWAS association (p=6.0e-12) | Major Consortium Study |
| rs547073714 | TANC1 | GWAS association (p=1.0e-11) | Major Consortium Study |
| rs542799569 | — | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs539384220 | — | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs377481824 | EPHB1 | GWAS association (p=3.0e-11) | Major Consortium Study |
| rs796390533 | GFRA2 | GWAS association (p=3.0e-11) | Major Consortium Study |
| rs557521042 | — | GWAS association (p=3.0e-11) | Major Consortium Study |
Associations aggregated from the GWAS Catalog and curated literature. Informational only — not medical advice.