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
10,966 positions on this site are linked to Height, out of 2,505,820 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
near IL27 · rs28698667
See detailed info → StandardTEX261 · rs2058552
See detailed info → StandardWWTR1 · rs1946704
See detailed info → StandardTSPAN15 · rs1227937
See detailed info → StandardPABPC4 · rs12028034
See detailed info → StandardRGS17 · rs655370
See detailed info → StandardCDC7 · rs13447526
See detailed info → StandardCROT · rs2051950
See detailed info → StandardCHD8 · rs10467770
See detailed info → StandardLINC00917 · rs12923579
See detailed info → StandardADAMTS17 · rs12443035
See detailed info → Standardnear MAPKAPK2 · rs4311892
See detailed info → StandardZFPL1 · rs35251366
See detailed info → Standardnear U6 · rs11945548
See detailed info → StandardSLC38A4-AS1 · rs11183521
See detailed info → Standardnear RPL31P32 · rs10944077
See detailed info → StandardNPR3 · rs55665822
See detailed info → StandardACAN · rs2280468
See detailed info → Standardnear Metazoa_SRP · rs959652
See detailed info → StandardGPATCH2 · rs7522803
See detailed info →Showing 20 of 10966 · page 161 of 549
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.