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 2,505,240 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
UMAD1 · rs7808919
See detailed info → StandardZNF76 · rs743965
See detailed info → StandardCCNT1 · rs7297499
See detailed info → StandardFBN1 · rs7165060
See detailed info → StandardARHGAP26 · rs6580274
See detailed info → StandardPELO-AS1 · rs4865535
See detailed info → StandardDAGLB · rs4720675
See detailed info → StandardSCIN · rs4555989
See detailed info → StandardCDH15 · rs3785415
See detailed info → StandardPMF1 · rs2758603
See detailed info → StandardSLC2A1 · rs17387775
See detailed info → Standardnear LINC00393 · rs17290172
See detailed info → StandardTRAP1 · rs1639150
See detailed info → StandardSCMH1-DT · rs147082624
See detailed info → StandardLYPLAL1-DT · rs12024289
See detailed info → Standardnear H3P24 · rs11750906
See detailed info → StandardTCF7L2 · rs11196236
See detailed info → StandardINPP1 · rs7592352
See detailed info → StandardGINS1 · rs2500406
See detailed info → StandardGLDN · rs2445738
See detailed info →Showing 20 of 10923 · page 147 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.