Trait
SNPs associated with Benign Chondrogenic Neoplasm
9 genetic variants across 6 genes have been associated with Benign Chondrogenic Neoplasm in published research. Key genes include ARHGAP20, GRXCR2, LOC105369698.
Associated variants9 total
| rsid | Gene | Effect | Evidence |
|---|---|---|---|
| rs145011008 | RBM45 | GWAS association (p=1.0e-13) | Major Consortium Study |
| rs118137644 | — | GWAS association (p=2.0e-13) | Major Consortium Study |
| rs185990766 | — | GWAS association (p=1.0e-12) | Major Consortium Study |
| rs190979921 | — | GWAS association (p=7.0e-12) | Major Consortium Study |
| rs565301439 | LOC105369698 | GWAS association (p=7.0e-12) | Major Consortium Study |
| rs138162229 | ARHGAP20 | GWAS association (p=8.0e-12) | Major Consortium Study |
| rs182407566 | SIPA1L2 | GWAS association (p=9.0e-12) | Major Consortium Study |
| rs753281643 | GRXCR2 | GWAS association (p=2.0e-11) | Major Consortium Study |
| rs185288821 | LTA | GWAS association (p=2.0e-11) | Major Consortium Study |
Associations aggregated from the GWAS Catalog and curated literature. Informational only — not medical advice.