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
11,375 positions on this site are linked to Height, out of 2,508,576 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
near ERCC6L2 · rs4743559
See detailed info → StandardCPED1 · rs4731006
See detailed info → StandardZNF160 · rs329701
See detailed info → StandardSEPTIN8 · rs256871
See detailed info → StandardDDX21 · rs17556220
See detailed info → StandardCNN3-DT · rs17407908
See detailed info → StandardMOCS2 · rs153602
See detailed info → StandardGUSBP5 · rs11100851
See detailed info → StandardKYAT1 · rs10988134
See detailed info → StandardSLIT2 · rs9992559
See detailed info → Standardnear SEPHS1P2 · rs875064
See detailed info → StandardGUSBP5 · rs7661384
See detailed info → StandardLINC01339 · rs702844
See detailed info → StandardPMPCB · rs6971734
See detailed info → StandardEML4 · rs6713242
See detailed info → Standardnear PPIAP39 · rs4918827
See detailed info → StandardSLC6A3 · rs2455391
See detailed info → StandardPEX7 · rs2295592
See detailed info → StandardLINC01517 · rs1761987
See detailed info → Standardnear GNAI2P1 · rs17221259
See detailed info →Showing 20 of 11375 · page 522 of 569
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.