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
10,923 positions on this site are linked to Height, out of 2,505,333 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
TCP11 · rs6934818
See detailed info → StandardBCL2L2 · rs3210043
See detailed info → StandardSERPINH1 · rs659418
See detailed info → StandardHMGA2 · rs12371967
See detailed info → StandardTRAF7 · rs2078282
See detailed info → StandardRP11-51F16.1 · rs11542436
See detailed info → StandardJAZF1 · rs73091214
See detailed info → StandardFAM184B · rs2109045
See detailed info → StandardFOXP1 · rs7647190
See detailed info → StandardGDF5OS · rs137874109
See detailed info → StandardHMGA2 · rs55981861
See detailed info → StandardPLAG1 · rs62515432
See detailed info → StandardRP11-600F24.7 · rs75482283
See detailed info → StandardFNDC3B · rs62281815
See detailed info → StandardRNY5 · rs80085026
See detailed info → StandardJAZF1 · rs1635851
See detailed info → StandardADAP2 · rs35958868
See detailed info → StandardRPS26P45 · rs10878984
See detailed info → StandardFAM83C · rs6060347
See detailed info → StandardDIS3L2 · rs111551994
See detailed info →Showing 20 of 10923 · page 541 of 547
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.