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
10,966 positions on this site are linked to Height, out of 2,505,820 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
PCSK5 · rs1416552
See detailed info → StandardLINC02240 · rs13162223
See detailed info → StandardLYPLAL1-DT · rs6541146
See detailed info → Standardnear LINC01738 · rs2457057
See detailed info → Standardnear HLF · rs1477143
See detailed info → StandardTIMELESS · rs774049
See detailed info → StandardADAM12 · rs1278337
See detailed info → StandardTHSD4 · rs11072297
See detailed info → StandardGLI2 · rs7582470
See detailed info → Standardnear PREX1 · rs4810829
See detailed info → StandardLINC03003 · rs2024679
See detailed info → Standardnear DLX5 · rs1207731
See detailed info → StandardDDAH1 · rs11161635
See detailed info → StandardARHGEF3 · rs9311618
See detailed info → StandardCDK6 · rs2282986
See detailed info → StandardFOXP1 · rs2121783
See detailed info → StandardMECOM · rs1048604
See detailed info → StandardTSPAN33 · rs919551
See detailed info → StandardSPATA20 · rs878619
See detailed info → Standardnear ECE1 · rs3026792
See detailed info →Showing 20 of 10966 · page 160 of 549
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.