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
11,679 positions on this site are linked to Height, out of 2,512,094 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 ACE3P · rs8075924
See detailed info → StandardCYP19A1 · rs10519301
See detailed info → Standardnear ROR2 · rs16907585
See detailed info → StandardYRDC · rs3795494
See detailed info → StandardGMDS · rs7751738
See detailed info → StandardAGXT · rs12695032
See detailed info → StandardMRPL42 · rs9943803
See detailed info → Standardnear MIR30B · rs7827871
See detailed info → Standardnear RPS4XP9 · rs9385404
See detailed info → Standardnear RN7SKP93 · rs6716309
See detailed info → Standardnear MIR17HG · rs9589196
See detailed info → StandardMAP4 · rs2230169
See detailed info → StandardBABAM2 · rs7558946
See detailed info → StandardCLASP2 · rs6796857
See detailed info → StandardSTAG1-DT · rs1533445
See detailed info → StandardH2BC6 · rs17533076
See detailed info → StandardCOLGALT2 · rs9970117
See detailed info → Standardnear MC3R · rs6064361
See detailed info → StandardCHD1L · rs9661159
See detailed info → StandardMED13L · rs7969182
See detailed info →Showing 20 of 11679 · page 56 of 584
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.