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
10,923 positions on this site are linked to Height, out of 2,505,333 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
ZNF318 · rs7742789
See detailed info → StandardPTPN9 · rs12904319
See detailed info → StandardDROSHA · rs112226333
See detailed info → StandardECD · rs7905296
See detailed info → StandardDIRC3 · rs2553033
See detailed info → StandardTBX4 · rs113121081
See detailed info → StandardNCOA2 · rs2926701
See detailed info → StandardSLC4A3 · rs11677783
See detailed info → StandardWDR70 · rs6883388
See detailed info → StandardRGS5 · rs76121963
See detailed info → StandardDYM · rs11659570
See detailed info → StandardAC005152.3 · rs116878242
See detailed info → StandardSUZ12P1 · rs113900126
See detailed info → StandardNDUFS3 · rs11605348
See detailed info → StandardEFEMP1 · rs58754091
See detailed info → StandardFGFR4 · rs2011077
See detailed info → StandardSLC35D2 · rs7020954
See detailed info → StandardRP11-63E9.1 · rs13213884
See detailed info → StandardACAN · rs35148461
See detailed info → StandardFER1L4 · rs57545942
See detailed info →Showing 20 of 10923 · page 540 of 547
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.