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
11,659 positions on this site are linked to Height, out of 2,511,894 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
FRY · rs17077100
See detailed info → Standardnear FAR2 · rs12821495
See detailed info → StandardCNBD2 · rs6060741
See detailed info → StandardSTK10 · rs4868136
See detailed info → StandardCPPED1 · rs2865895
See detailed info → StandardMECOM · rs16854266
See detailed info → Standardnear FAM76B · rs10831389
See detailed info → StandardBRD3 · rs10993907
See detailed info → StandardAGO2 · rs1060832
See detailed info → StandardPUM2 · rs10182834
See detailed info → Standardnear ICA1 · rs9655062
See detailed info → StandardRNF130 · rs4130025
See detailed info → StandardSEPTIN9 · rs2002573
See detailed info → Standardnear MAN1C1 · rs807250
See detailed info → StandardDRAM1 · rs4764841
See detailed info → StandardTMEM50A · rs3091242
See detailed info → Standardnear EXOSC9 · rs56077950
See detailed info → Standardnear BMP6 · rs10793850
See detailed info → StandardPRKG2 · rs710839
See detailed info → StandardROCR · rs17767924
See detailed info →Showing 20 of 11659 · page 37 of 583
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.