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
11,639 positions on this site are linked to Height, out of 2,511,480 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
near PTCH1 · rs10120219
See detailed info → Standardnear SIK3 · rs12269901
See detailed info → StandardPRKG2 · rs1662837
See detailed info → StandardCNOT4 · rs17480616
See detailed info → StandardDR1 · rs1559828
See detailed info → StandardCXXC5 · rs3822742
See detailed info → Standardnear GH2 · rs2955250
See detailed info → StandardADAMTSL3 · rs10520573
See detailed info → Standardnear DIDO1 · rs747680
See detailed info → StandardLTBP2 · rs862041
See detailed info → Standardnear LINC00917 · rs8054549
See detailed info → Standardnear C17orf67 · rs12602666
See detailed info → StandardAIP · rs12795957
See detailed info → Standardnear MYH7 · rs11621360
See detailed info → Standardnear WNT4 · rs7521902
See detailed info → StandardCARMIL1 · rs214057
See detailed info → Standardnear PRKG2 · rs1443536
See detailed info → StandardFBXW8 · rs7302025
See detailed info → StandardADAMTS10 · rs8108747
See detailed info → StandardSERPINE2 · rs12436
See detailed info →Showing 20 of 11639 · page 19 of 582
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.