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
11,114 positions on this site are linked to Height, out of 2,506,432 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
CTU2 · rs8059048
See detailed info → StandardDIS3L2 · rs6728302
See detailed info → StandardSMOC2 · rs2342646
See detailed info → StandardFMNL1-DT · rs17630064
See detailed info → StandardAMZ1 · rs798557
See detailed info → StandardLETR1 · rs12912439
See detailed info → Standardnear CRYAB · rs12808601
See detailed info → Standardnear ATP5MC2 · rs10876470
See detailed info → StandardADAMTS17 · rs746711
See detailed info → Standardnear IGFBP4 · rs584828
See detailed info → StandardSPDEF · rs75149985
See detailed info → StandardTGFB2 · rs1418553
See detailed info → StandardPPP2R2D · rs9419374
See detailed info → Standardnear LMAN2L · rs6746896
See detailed info → Standardnear SNED1 · rs4344930
See detailed info → StandardNALCN-AS1 · rs8922
See detailed info → Standardnear UPF3A · rs7998612
See detailed info → StandardCCDC80 · rs6807798
See detailed info → StandardATP6V0D1 · rs2279023
See detailed info → Standardnear ISG20 · rs6496519
See detailed info →Showing 20 of 11114 · page 192 of 556
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.