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
11,159 positions on this site are linked to Height, out of 2,506,722 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
KIZ · rs2252720
See detailed info → StandardARID5B · rs4245597
See detailed info → Standardnear LINC02058 · rs34509
See detailed info → StandardCREBRF · rs3095844
See detailed info → StandardNFIC · rs55805295
See detailed info → StandardEPAS1 · rs4953353
See detailed info → Standardnear GRP · rs7230581
See detailed info → StandardEHD3 · rs649729
See detailed info → StandardCOLGALT2 · rs114661926
See detailed info → StandardHES7 · rs8067165
See detailed info → StandardH1-10-AS1 · rs4073154
See detailed info → StandardCLEC4M · rs874492
See detailed info → StandardDLX6-AS1 · rs56363908
See detailed info → StandardGPC5 · rs7319045
See detailed info → Standardnear DCUN1D4 · rs2102278
See detailed info → StandardMORC3 · rs113382956
See detailed info → StandardBRD3 · rs2520099
See detailed info → StandardREEP5 · rs153560
See detailed info → StandardDCST1 · rs74520550
See detailed info → StandardLTBP1 · rs6714546
See detailed info →Showing 20 of 11159 · page 221 of 558
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.