Trait
SNPs associated with Peyronie disease
17 genetic variants across 7 genes have been associated with Peyronie disease in published research. Key genes include CDNF, FOXP1, GLT6D1.
Associated variants17 total
| rsid | Gene | Effect | Evidence |
|---|---|---|---|
| rs12706146 | — | GWAS association (p=6.0e-40) | Major Consortium Study |
| rs10226248 | — | GWAS association (p=1.0e-37) | Major Consortium Study |
| rs528539364 | FOXP1 | GWAS association (p=9.0e-14) | Major Consortium Study |
| rs143888834 | — | GWAS association (p=4.0e-13) | Major Consortium Study |
| rs1040551 | — | GWAS association (p=5.0e-13) | Major Consortium Study |
| rs556089591 | GLT6D1 | GWAS association (p=4.0e-12) | Major Consortium Study |
| rs530928701 | — | GWAS association (p=6.0e-12) | Major Consortium Study |
| rs370193349 | — | GWAS association (p=9.0e-12) | Major Consortium Study |
| rs555372783 | WDR61 | GWAS association (p=1.0e-11) | Major Consortium Study |
| rs550348651 | — | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs1239296705 | SPTLC2 | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs574927914 | ZFP90 | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs1051993455 | CDNF | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs1840496 | — | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs374153640 | — | GWAS association (p=4.0e-11) | Major Consortium Study |
| rs28971325 | WNT7B | GWAS association (p=3.0e-26) | Major Consortium Study |
| rs6054308 | — | GWAS association (p=3.0e-13) | Major Consortium Study |
Associations aggregated from the GWAS Catalog and curated literature. Informational only — not medical advice.