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
11,426 positions on this site are linked to Height, out of 2,509,091 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
FAM184B · rs2109045
See detailed info → StandardJAZF1 · rs73091214
See detailed info → StandardRNY5 · rs80085026
See detailed info → StandardJAZF1 · rs1635851
See detailed info → StandardADAP2 · rs35958868
See detailed info → StandardFNDC3B · rs62281815
See detailed info → StandardFAM83C · rs6060347
See detailed info → StandardPXYLP1 · rs28721484
See detailed info → StandardC6orf106 · rs2814973
See detailed info → StandardRPS26P45 · rs10878984
See detailed info → StandardDIS3L2 · rs111551994
See detailed info → StandardTLE3 · rs4777230
See detailed info → StandardDLEU1 · rs1568672
See detailed info → StandardPRKG2 · rs1975474
See detailed info → StandardRILPL2 · rs28376121
See detailed info → StandardACAN · rs16942323
See detailed info → Standardnear UQCC1 · rs6060402
See detailed info → Standardnear PPP1R3A · rs184469050
See detailed info → StandardRP1-35C21.2 · rs146949893
See detailed info → StandardCMTM8 · rs6765866
See detailed info →Showing 20 of 11426 · page 563 of 572
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.