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
10,796 positions on this site are linked to Height, out of 2,501,195 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
CPLANE1 · rs301904
See detailed info → StandardPTPN21 · rs2274735
See detailed info → StandardHAS3 · rs2232229
See detailed info → StandardMKLN1 · rs1979567
See detailed info → StandardH2AZ1-DT · rs17620559
See detailed info → StandardRAI14 · rs17522675
See detailed info → Standardnear SLC28A3 · rs1246326
See detailed info → Standardnear KCNJ2-AS1 · rs9915368
See detailed info → StandardEXOSC3 · rs927631
See detailed info → Standardnear GHRHR · rs881499
See detailed info → StandardZFAT · rs7812708
See detailed info → StandardUMAD1 · 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 →Showing 20 of 10796 · page 143 of 540
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.