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
11,969 positions on this site are linked to Height, out of 2,518,705 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
ATAD5 · rs11651858
See detailed info → StandardE2F7 · rs10862960
See detailed info → StandardAOPEP · rs1004813
See detailed info → StandardPRKG1 · rs9988728
See detailed info → StandardNCOA7 · rs7754833
See detailed info → Standardnear TRIM41 · rs17080884
See detailed info → StandardPCNA · rs8125170
See detailed info → StandardCTIF · rs16949934
See detailed info → Standardnear TMEM171 · rs13179315
See detailed info → StandardCREB5 · rs1964240
See detailed info → StandardLINC02680 · rs1979720
See detailed info → StandardNUDT5 · rs2399786
See detailed info → StandardPELATON · rs17196808
See detailed info → Standardnear SSTR5 · rs174643
See detailed info → StandardUBE3D · rs11758364
See detailed info → Standardnear RN7SL720P · rs10962813
See detailed info → StandardADAMTSL3 · rs899926
See detailed info → StandardCCDC91 · rs11049502
See detailed info → StandardCPSF3 · rs10929582
See detailed info → StandardRB1 · rs4151450
See detailed info →Showing 20 of 11969 · page 51 of 599
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.