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 C12orf42 · rs149580590
See detailed info → Standardnear TXNRD1 · rs191631370
See detailed info → StandardSTAB2 · rs187503377
See detailed info → StandardSTAB2 · rs190613886
See detailed info → StandardF5 · rs1557570
See detailed info → StandardCXCL1 · rs74544699
See detailed info → Standardnear ME1 · rs2324229
See detailed info → StandardMYO19 · rs76842834
See detailed info → Standardnear FAM124B · rs13024765
See detailed info → Standardnear TM2D3 · rs112967753
See detailed info → Standardnear TBC1D3B · rs142499028
See detailed info → StandardMYO19 · rs184920307
See detailed info → StandardPCSK6 · rs4965869
See detailed info → StandardCCR3 · rs79815064
See detailed info → StandardSPINK8 · rs74735576
See detailed info → Standardnear PTH1R · rs138662258
See detailed info → StandardKIF15 · rs143612100
See detailed info → StandardPOC1A · rs77861329
See detailed info → Standardnear ZNF852 · rs73072664
See detailed info → StandardDOCK3 · rs76761409
See detailed info →Showing 20 of 79 · page 2 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.