Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license
646 positions on this site are linked to Monocyte Count, out of 2,507,434 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense
ZNF516 · rs3177609
See detailed info → Standardnear GATA6 · rs28631485
See detailed info → Standardnear KCNJ2 · rs28688305
See detailed info → StandardFANCA · rs11646229
See detailed info → StandardXPO6 · rs4788046
See detailed info → StandardPKD1 · rs34197769
See detailed info → StandardDLST · rs2300598
See detailed info → StandardIPO8 · rs4082413
See detailed info → StandardLMO2 · rs1885525
See detailed info → Standardnear PTEN · rs79252156
See detailed info → Standardnear IPMK · rs1698403
See detailed info → StandardPALM2AKAP2 · rs4978866
See detailed info → StandardNSMCE2 · rs2385094
See detailed info → StandardZFPM2 · rs2343592
See detailed info → Standardnear LYN · rs333613
See detailed info → Standardnear POTEA · rs117148746
See detailed info → Standardnear CTSB · rs57928712
See detailed info → Standardnear MED13L · rs73204034
See detailed info → StandardKLRC1 · rs7298732
See detailed info → Standardnear CDC5L · rs75492293
See detailed info →Showing 20 of 646 · page 32 of 33
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.