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
10,966 positions on this site are linked to Height, out of 2,505,820 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
JAZF1 · rs6958010
See detailed info → StandardHHIP · rs6854783
See detailed info → StandardTGFB2 · rs6657275
See detailed info → StandardPAPPA2 · rs6656137
See detailed info → StandardCASC20 · rs6117303
See detailed info → Standardnear CASC20 · rs6117253
See detailed info → StandardEDEM2 · rs6088728
See detailed info → StandardCRADD · rs4761739
See detailed info → Standardnear RYBP · rs4677156
See detailed info → StandardFGFR4 · rs442856
See detailed info → StandardPRKG2 · rs3114135
See detailed info → StandardESR1 · rs3020411
See detailed info → StandardPCBD2 · rs299364
See detailed info → StandardRAB26 · rs258281
See detailed info → StandardCYP19A1 · rs2305707
See detailed info → StandardBCAS3 · rs2286530
See detailed info → StandardKLHL29 · rs1991083
See detailed info → StandardCABLES1 · rs17186875
See detailed info → StandardCRADD · rs1471816
See detailed info → Standardnear C17orf67 · rs1401796
See detailed info →Showing 20 of 10966 · page 548 of 549
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.