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
C14orf39 · 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 → Standardnear NACA2 · rs78031430
See detailed info → StandardLILRB2 · rs77679745
See detailed info → Standardnear RNU6-295P · rs75447677
See detailed info → StandardNBL1 · rs7523192
See detailed info → StandardCCDC8 · rs75175362
See detailed info → StandardPRR34 · rs7510754
See detailed info → Standardnear KCNC2 · rs7314533
See detailed info → StandardDYM · rs72921677
See detailed info → Standardnear JADRR · rs72681619
See detailed info → Standardnear U3 · rs7093041
See detailed info → StandardGALNT7-DT · rs6855544
See detailed info →Showing 20 of 11344 · page 233 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.