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 2,511,526 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 LINC02995 · rs17738166
See detailed info → Standardnear COL8A1 · rs1014514
See detailed info → StandardGNAS · rs2057291
See detailed info → StandardRILPL2 · rs28481863
See detailed info → StandardSKI · rs12743493
See detailed info → StandardZNF638 · rs3771371
See detailed info → StandardLPP · rs6787621
See detailed info → StandardCDK12 · rs6503521
See detailed info → StandardATAD5 · rs76947600
See detailed info → StandardCASC15 · rs196051
See detailed info → StandardADGRG6 · rs1040525
See detailed info → Standardnear N4BP2 · rs794016
See detailed info → StandardADAMTS10 · rs7249094
See detailed info → StandardLCORL · rs724577
See detailed info → StandardPAPPA · rs7027103
See detailed info → StandardPDE3A · rs6487088
See detailed info → StandardGHR · rs17574650
See detailed info → StandardDOT1L · rs12983357
See detailed info → Standardnear PCSK5 · rs3814115
See detailed info → StandardTPCN2 · rs1060435
See detailed info →Showing 20 of 11639 · page 22 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.