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
11,344 positions on this site are linked to Height, out of 2,508,301 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
TTBK2 · rs66530524
See detailed info → Standardnear RNA5SP455 · rs6507549
See detailed info → StandardMLF2 · rs6489734
See detailed info → Standardnear FST · rs62357775
See detailed info → StandardEFCC1 · rs62265318
See detailed info → StandardWDR81 · rs62090043
See detailed info → Standardnear RBL1 · rs568740796
See detailed info → Standardnear U3 · rs56052727
See detailed info → StandardZNF521 · rs56044429
See detailed info → StandardADAMTSL3 · rs536785166
See detailed info → StandardLINC01755 · rs4926705
See detailed info → StandardTWIST1 · rs4721746
See detailed info → StandardMOCS1 · rs41273140
See detailed info → Standardnear GNL1 · rs41265836
See detailed info → Standardnear CST5 · rs4074167
See detailed info → StandardNRXN2-AS1 · rs3825074
See detailed info → StandardCUX1 · rs366345
See detailed info → StandardMAP2K1 · rs34842367
See detailed info → StandardYJU2B · rs346172
See detailed info → StandardLINC00620 · rs34325349
See detailed info →Showing 20 of 11344 · page 234 of 568
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.