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
11,696 positions on this site are linked to Height, out of 2,512,366 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
ESR1 · rs2982570
See detailed info → StandardIRAIN · rs1991211
See detailed info → StandardPTPRJ · rs1681630
See detailed info → Standardnear ZNF483 · rs10980921
See detailed info → Standardnear SOCS2 · rs10859538
See detailed info → StandardRUFY4 · rs6726126
See detailed info → StandardDNM3 · rs3817924
See detailed info → StandardCSMD1 · rs2688325
See detailed info → StandardCCDC171 · rs3008705
See detailed info → StandardZHX2 · rs2833
See detailed info → StandardGLI2 · rs13392139
See detailed info → StandardCSTPP1 · rs117128752
See detailed info → Standardnear MTCO1P24 · rs116075081
See detailed info → Standardnear LINC00485 · rs10860909
See detailed info → Standardnear CCDC162P · rs1074765
See detailed info → StandardIL16 · rs931963
See detailed info →Showing 16 of 11696 · page 585 of 585
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.