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
11,639 positions on this site are linked to Height, out of 2,511,480 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
LPP · rs4686991
See detailed info → StandardTHOC1 · rs8087639
See detailed info → Standardnear HLA-DQA1 · rs9271348
See detailed info → StandardITGB8 · rs1023522
See detailed info → StandardSMAD6 · rs7179372
See detailed info → StandardLRRC69 · rs4339600
See detailed info → StandardSENP2 · rs3087964
See detailed info → Standardnear TBX2-AS1 · rs11868532
See detailed info → StandardDOT1L · rs12982744
See detailed info → Standardnear PSCA · rs2976397
See detailed info → Standardnear NHEJ1 · rs359974
See detailed info → StandardHSPG2 · rs9426785
See detailed info → StandardCCND2 · rs3217844
See detailed info → StandardPVT1 · rs4733789
See detailed info → StandardLCORL · rs6842114
See detailed info → Standardnear BLTP3A · rs55635636
See detailed info → Standardnear U6 · rs28783740
See detailed info → StandardCAPZB · rs10917452
See detailed info → StandardHCG27 · rs10807081
See detailed info → StandardVGLL3 · rs1836918
See detailed info →Showing 20 of 11639 · page 14 of 582
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.