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
11,645 positions on this site are linked to Height, out of 2,511,803 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 PSMB3P2 · rs17496232
See detailed info → StandardFCHO2 · rs16878881
See detailed info → Standardnear LINC02004 · rs6439474
See detailed info → StandardRGL1 · rs4132276
See detailed info → StandardHAS3 · rs2232227
See detailed info → StandardTFDP2 · rs7642874
See detailed info → StandardCHD9 · rs8058720
See detailed info → Standardnear ACAN · rs4932412
See detailed info → Standardnear LPGAT1 · rs3862952
See detailed info → Standardnear HLA-DQA1 · rs9271574
See detailed info → StandardPTPN9 · rs7163907
See detailed info → StandardCDC25A · rs3731494
See detailed info → StandardKCNQ1 · rs2283200
See detailed info → StandardCEP112 · rs1833347
See detailed info → StandardLINC02895 · rs17639328
See detailed info → StandardIGF1R · rs12898337
See detailed info → Standardnear SCP2D1-AS1 · rs6132147
See detailed info → StandardANTXR1 · rs4854538
See detailed info → StandardTSPAN9 · rs11062585
See detailed info → StandardRSRC1 · rs4411841
See detailed info →Showing 20 of 11645 · page 32 of 583
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.