79 positions on this site are linked to MIP-1b (CCL4) Levels, out of 7,519 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near CACNA2D2 · rs183139656
See detailed info → StandardUSP4 · rs75394422
See detailed info → StandardCOL7A1 · rs76061303
See detailed info → StandardTMIE · rs112579976
See detailed info → Standardnear ABHD5 · rs137933720
See detailed info → StandardDAG1 · rs115970881
See detailed info → StandardMON1A · rs140867372
See detailed info → StandardSCAP · rs77215549
See detailed info → Standardnear TOPAZ1 · rs142242702
See detailed info → StandardMAP4 · rs75485436
See detailed info → Standardnear RBM5 · rs115192074
See detailed info → StandardIP6K2 · rs62261476
See detailed info → StandardZDHHC3 · rs35142429
See detailed info → StandardIP6K1 · rs116238056
See detailed info → StandardZNF197 · rs140824699
See detailed info → StandardKIF9 · rs79062474
See detailed info → Standardnear HNF1B · rs7221878
See detailed info → StandardMRM1 · rs78943308
See detailed info → StandardACACA · rs185128671
See detailed info → StandardCCL4L1 · rs113877493
See detailed info →Showing 20 of 79 · page 3 of 4
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.