79 positions on this site are linked to MIP-1b (CCL4) Levels, out of 7,431 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CSMD1 · rs56367447
See detailed info → StandardSUSD2 · rs147224860
See detailed info → StandardEFHC1 · rs182429465
See detailed info → StandardECT2 · rs116467561
See detailed info → StandardTNFSF10 · rs79287178
See detailed info → StandardNCEH1 · rs73173340
See detailed info → Standardnear GAREM1 · rs189585165
See detailed info → Standardnear DTNA · rs72965213
See detailed info → Standardnear KLHL14 · rs138987090
See detailed info → StandardDTNA · rs144916876
See detailed info → Standardnear DSG1 · rs193112415
See detailed info → StandardB4GALT6 · rs62093514
See detailed info → StandardRNF125 · rs62093946
See detailed info → StandardMEP1B · rs192989810
See detailed info → StandardGAREM1 · rs112394247
See detailed info → Sensitivenear EPHA8 · rs75134464
See detailed info → StandardF5 · rs4656185
See detailed info → StandardCLEC11A · rs116924815
See detailed info → StandardSTAB2 · rs190613886
See detailed info → StandardSTAB2 · rs187503377
See detailed info →Showing 20 of 79 · page 1 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.