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
10,927 positions on this site are linked to Height, out of 2,505,721 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
C6orf106 · rs2814993
See detailed info → StandardGPR126 · rs3748069
See detailed info → StandardNFATC2 · rs228836
See detailed info → StandardEXTL3 · rs10448080
See detailed info → StandardSLC17A2 · rs1865760
See detailed info → StandardJMJD4 · rs10799445
See detailed info → StandardCCDC108/IHH · rs12470505
See detailed info → StandardTLE3 · rs10152591
See detailed info → StandardATP5SL · rs17318596
See detailed info → StandardDIS3L2 · rs3103267
See detailed info → StandardRDHE2 · rs4075154
See detailed info → StandardLYPLAL1 · rs11118346
See detailed info → StandardADAM28 · rs1013209
See detailed info → StandardPCCB · rs9844666
See detailed info → StandardPEX2 · rs6473015
See detailed info → StandardHLA locus · rs6457620
See detailed info → StandardBOD1 · rs889014
See detailed info → StandardOR2J3 · rs3129109
See detailed info → StandardC3orf47 · rs6439167
See detailed info → StandardIGF2BP3 · rs12534093
See detailed info →Showing 20 of 10927 · page 543 of 547
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.