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
11,258 positions on this site are linked to Height, out of 2,507,547 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 PGP · rs27345
See detailed info → Standardnear EXOSC9 · rs6838153
See detailed info → Standardnear ZC3H11B · rs10746387
See detailed info → StandardCPZ · rs11723641
See detailed info → Standardnear L3MBTL3 · rs1337775
See detailed info → StandardCRADD · rs4761530
See detailed info → StandardNCAPG · rs16895802
See detailed info → StandardADCY9 · rs2230742
See detailed info → StandardEZH1 · rs11657684
See detailed info → StandardPVT1 · rs1902778
See detailed info → StandardFILIP1 · rs9360910
See detailed info → StandardHMGA2 · rs11834900
See detailed info → Standardnear LHX3 · rs11103372
See detailed info → Standardnear PBX4 · rs8113006
See detailed info → Standardnear LINC03007 · rs10238703
See detailed info → StandardDLEU7 · rs3118917
See detailed info → StandardINSR · rs12459488
See detailed info → StandardMIR193BHG · rs30232
See detailed info → StandardPIEZO1 · rs10775348
See detailed info → StandardIGF2BP2 · rs6765808
See detailed info →Showing 20 of 11258 · page 7 of 563
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.