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
11,639 positions on this site are linked to Height, out of 2,511,526 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
SPRY4-AS1 · rs253438
See detailed info → StandardPHF20 · rs2425163
See detailed info → StandardLMO7 · rs9318373
See detailed info → StandardAKT3 · rs14403
See detailed info → StandardRABGAP1 · rs803733
See detailed info → StandardSMG6-AS1 · rs16951881
See detailed info → StandardBMP6 · rs553291419
See detailed info → StandardSTPG4 · rs10460536
See detailed info → StandardDRAIC · rs88505
See detailed info → StandardSBNO2 · rs740495
See detailed info → StandardLTBP1 · rs218197
See detailed info → StandardH1-10-AS1 · rs6763292
See detailed info → StandardIGF2BP3 · rs11769151
See detailed info → StandardCOL12A1 · rs240724
See detailed info → StandardPSMD13 · rs2272566
See detailed info → StandardFAF1 · rs113836734
See detailed info → StandardTRIM6-TRIM34 · rs3751006
See detailed info → Standardnear TRIP11 · rs67015182
See detailed info → StandardEGR3-AS1 · rs2313167
See detailed info → StandardANKRD52 · rs72648137
See detailed info →Showing 20 of 11639 · page 1 of 582
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.