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
11,114 positions on this site are linked to Height, out of 2,506,525 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
ANO1 · rs3781660
See detailed info → StandardDAAM2 · rs456462
See detailed info → StandardPRKG2 · rs17556750
See detailed info → Standardnear KIF1B · rs3903151
See detailed info → Standardnear ISG20 · rs4534816
See detailed info → StandardRORB · rs1327827
See detailed info → StandardLINC01592 · rs10504440
See detailed info → StandardRPS10-NUDT3 · rs540105494
See detailed info → StandardPINLYP · rs2682587
See detailed info → StandardMYPN · rs1900016
See detailed info → Standardnear PRKG2 · rs62302280
See detailed info → StandardHOXD12 · rs847151
See detailed info → StandardTHBS3 · rs35154152
See detailed info → StandardIGFBP3 · rs6953668
See detailed info → Standardnear FAM76B · rs1255529
See detailed info → StandardMIR7-3HG · rs3760954
See detailed info → Standardnear LINC01713 · rs6038587
See detailed info → StandardTAF5 · rs57707166
See detailed info → StandardSLA2 · rs4810266
See detailed info → Standardnear SSBP3 · rs11206349
See detailed info →Showing 20 of 11114 · page 203 of 556
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.