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
11,323 positions on this site are linked to Height, out of 2,508,068 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
ADAM28 · rs1013209
See detailed info → StandardLYPLAL1 · rs11118346
See detailed info → StandardPCCB · rs9844666
See detailed info → StandardPEX2 · rs6473015
See detailed info → StandardHLA locus · rs6457620
See detailed info → StandardBOD1 · rs889014
See detailed info → StandardOR2J3 · rs3129109
See detailed info → StandardC3orf47 · rs6439167
See detailed info → StandardIGF2BP3 · rs12534093
See detailed info → StandardH6PD · rs6662509
See detailed info → StandardBMP6 · rs1885486
See detailed info → StandardFER · rs13177718
See detailed info → StandardMYO9A · rs12902421
See detailed info → StandardSTAT2 · rs2066807
See detailed info → StandardSENP6 · rs9360921
See detailed info → StandardC2orf52 · rs6750795
See detailed info → StandardPPARD/FANCE · rs6457821
See detailed info → StandardIPPK · rs9969804
See detailed info → StandardDNAJC27 · rs4665736
See detailed info → StandardNUCB2 · rs1330
See detailed info →Showing 20 of 11323 · page 565 of 567
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.