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
11,645 positions on this site are linked to Height, out of 2,511,803 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
MGAT1 · rs3733750
See detailed info → StandardDYM · rs2078286
See detailed info → StandardCAV2-DT · rs1918917
See detailed info → Standardnear PKDCC · rs12479347
See detailed info → Standardnear RN7SL396P · rs6981251
See detailed info → Standardnear RNA5SP455 · rs603354
See detailed info → StandardUST · rs2153252
See detailed info → StandardADAMTS17 · rs1383546
See detailed info → Standardnear LINC02409 · rs10860152
See detailed info → StandardLNX1 · rs6855607
See detailed info → Standardnear RPL23AP44 · rs4385235
See detailed info → StandardZBTB20 · rs9855047
See detailed info → StandardNUP153 · rs6927877
See detailed info → StandardTSPO · rs6972
See detailed info → StandardCADPS2 · rs17463319
See detailed info → Standardnear TUG1 · rs4820921
See detailed info → StandardRGL1 · rs11591089
See detailed info → StandardREPS1 · rs973170
See detailed info → StandardZFHX3 · rs4887925
See detailed info → StandardCOL6A3 · rs2645772
See detailed info →Showing 20 of 11645 · page 31 of 583
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.