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
11,493 positions on this site are linked to Height, out of 2,509,702 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
ZIM2 · rs7256072
See detailed info → StandardMESD · rs7178551
See detailed info → StandardSH3GL3 · rs7173804
See detailed info → Standardnear TMEM174 · rs71636072
See detailed info → StandardGARNL3 · rs71481314
See detailed info → StandardAAMDC · rs7119332
See detailed info → StandardLINC02488 · rs710400
See detailed info → StandardSPON1 · rs7102710
See detailed info → StandardMTMR7 · rs7009094
See detailed info → StandardANKH · rs697568
See detailed info → StandardHDAC9 · rs6950376
See detailed info → StandardLINC02900 · rs6896456
See detailed info → StandardPAM · rs6885642
See detailed info → StandardSORBS2 · rs6858040
See detailed info → StandardSPOCK3 · rs6817936
See detailed info → StandardTNNT1 · rs67795913
See detailed info → Standardnear RN7SKP224 · rs6739811
See detailed info → Standardnear SMASR · rs66717113
See detailed info → StandardMS4A4E · rs666555
See detailed info → StandardARAP3 · rs6580194
See detailed info →Showing 20 of 11493 · page 310 of 575
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.