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
11,159 positions on this site are linked to Height, out of 2,506,722 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
CYP19A1 · rs28566535
See detailed info → StandardMEF2C · rs10037512
See detailed info → StandardADAMTSL3 · rs8024628
See detailed info → Standardnear CTDSP2 · rs10747787
See detailed info → Standardnear FGFR1 · rs881301
See detailed info → StandardCHD4 · rs7310535
See detailed info → StandardFGFR4 · rs422421
See detailed info → StandardAMZ1 · rs798491
See detailed info → StandardANKS1A · rs13210323
See detailed info → StandardHOXD3 · rs4972504
See detailed info → Standardnear ADAMTS3 · rs4694504
See detailed info → StandardC14orf39 · rs1254276
See detailed info → StandardMKL2 · rs1659127
See detailed info → StandardHMGA1 · rs10807138
See detailed info → StandardPPP1CA · rs61734601
See detailed info → StandardPARK2 · rs9456748
See detailed info → StandardZBTB21 · rs915837
See detailed info → StandardSLC27A2 · rs8032718
See detailed info → StandardDENND1A · rs79565874
See detailed info → StandardRNF207 · rs79344881
See detailed info →Showing 20 of 11159 · page 222 of 558
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.