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 2,505,381 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
RGP1 · rs1322045
See detailed info → StandardNFATC4 · rs11628929
See detailed info → StandardSLC2A2 · rs11711206
See detailed info → StandardSLC22A3 · rs518295
See detailed info → StandardTBX15 · rs1779454
See detailed info → StandardTMC3-AS1 · rs62035353
See detailed info → Standardnear BMP6 · rs6927500
See detailed info → StandardMACROD2 · rs16996637
See detailed info → StandardPAMR1 · rs644755
See detailed info → StandardNEDD4 · rs1863758
See detailed info → StandardZNF710 · rs2970357
See detailed info → StandardRREB1 · rs7743323
See detailed info → StandardRAB3GAP1 · rs115227414
See detailed info → StandardMTOR · rs1148480
See detailed info → Standardnear ZFP36L1 · rs7146217
See detailed info → StandardDISP1 · rs139405583
See detailed info → StandardMYO9B · rs2305769
See detailed info → StandardCCDC26 · rs4636162
See detailed info → StandardPARP1 · rs932002
See detailed info → StandardFGL1 · rs10099622
See detailed info →Showing 20 of 10923 · page 536 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.