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.
LIG3 · rs145583519
See detailed info → Standardnear TBC1D3B · rs144563201
See detailed info → StandardMMP28 · rs76960253
See detailed info → Standardnear TMEM132E · rs72829264
See detailed info → Standardnear UNC45B · rs1994089
See detailed info → StandardGRK6 · rs1801020
See detailed info → StandardSDAD1 · rs55876513
See detailed info → StandardEPHA8 · rs45498698
See detailed info → StandardSEC22C · rs114202043
See detailed info → Standardnear GASK1A · rs116826172
See detailed info → StandardCCDC13 · rs115333627
See detailed info → StandardACKR2 · rs2228467
See detailed info → Standardnear CCL24 · rs2024050
See detailed info → StandardOR10J1 · rs4656236
See detailed info → StandardHGFAC · rs3748034
See detailed info → Standardnear KCTD15 · rs28637706
See detailed info → StandardIL11RA · rs2070074
See detailed info → StandardCXCL10 · rs141053179
See detailed info → Standardnear PARM1 · rs113831257
See detailed info →Showing 19 of 79 · page 4 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.