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
10,926 positions on this site are linked to Height, out of 2,505,576 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
PEMT · rs4646359
See detailed info → StandardZBTB38 · rs4683404
See detailed info → StandardGRB10 · rs2299156
See detailed info → StandardTCF4 · rs2958183
See detailed info → StandardLINC00446 · rs7992650
See detailed info → Standardnear CAPZA2 · rs12706121
See detailed info → StandardANAPC10 · rs6823268
See detailed info → StandardASB7 · rs1873958
See detailed info → Standardnear LINC01734 · rs6129229
See detailed info → StandardIER2 · rs1042164
See detailed info → StandardDSE · rs6907315
See detailed info → Standardnear ACSBG1 · rs12916463
See detailed info → StandardPRKCZ · rs262654
See detailed info → StandardLINC02715 · rs7113219
See detailed info → Standardnear QKI · rs73029259
See detailed info → StandardAFAP1 · rs56411722
See detailed info → StandardPHC1 · rs1805737
See detailed info → Standardnear TENT4A · rs274668
See detailed info → Standardnear LINC03006 · rs71564907
See detailed info → StandardEXOSC5 · rs878083
See detailed info →Showing 20 of 10926 · page 535 of 547
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.