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
11,083 positions on this site are linked to Height, out of 2,506,337 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
COL6A5 · rs4688801
See detailed info → StandardMRC2 · rs2014055
See detailed info → Standardnear ANAPC10 · rs114364021
See detailed info → Standardnear H19 · rs74764171
See detailed info → Standardnear TUBB · rs56026300
See detailed info → StandardBMP2 · rs17721822
See detailed info → StandardRPSAP52 · rs9669644
See detailed info → StandardZFAT · rs7000796
See detailed info → StandardAAMDC · rs2051484
See detailed info → StandardDNMT3A · rs137926936
See detailed info → StandardCDC14B · rs7852498
See detailed info → StandardHELLPAR · rs74900775
See detailed info → StandardSCAMP5 · rs3812945
See detailed info → StandardHLA-DQA1 · rs150752156
See detailed info → StandardNBEAL2 · rs73075647
See detailed info → Standardnear PIK3R1 · rs11750646
See detailed info → Standardnear MIR422A · rs11631933
See detailed info → StandardZNF76 · rs6919534
See detailed info → StandardDNAJC27 · rs62140616
See detailed info → StandardSH2D5 · rs113664832
See detailed info →Showing 20 of 11083 · page 186 of 555
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.