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 2,512,183 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
CTNNB1 · rs11711946
See detailed info → StandardPDE8A · rs12900078
See detailed info → StandardTIAM2 · rs11751128
See detailed info → StandardFKBP5 · rs13192954
See detailed info → StandardMAP6 · rs11236476
See detailed info → StandardFAM184B · rs12642968
See detailed info → Standardnear HMG20A · rs1317320
See detailed info → StandardTGFB2 · rs11466412
See detailed info → StandardSPOCD1 · rs12737935
See detailed info → StandardAOPEP · rs12337992
See detailed info → StandardARID5B · rs4506592
See detailed info → StandardITPR3 · rs10947427
See detailed info → StandardLUZP1 · rs6663369
See detailed info → Standardnear SETD9 · rs832539
See detailed info → StandardPENK-AS1 · rs2609996
See detailed info → StandardMYO9A · rs2291276
See detailed info → StandardRPL34-DT · rs6835794
See detailed info → Standardnear CYTL1 · rs9998195
See detailed info → StandardOS9-AS1 · rs7979246
See detailed info → Standardnear U6 · rs2540844
See detailed info →Showing 20 of 11679 · page 57 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.