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
10,923 positions on this site are linked to Height, out of 2,505,333 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
XRCC1 · rs2293036
See detailed info → StandardLDB3 · rs1986382
See detailed info → StandardLCORL · rs13102976
See detailed info → StandardPACSIN1 · rs7748484
See detailed info → Standardnear LINC02120 · rs7730787
See detailed info → StandardARID1B · rs6907209
See detailed info → StandardSEC31B · rs3750629
See detailed info → Standardnear CHST11 · rs2248343
See detailed info → Standardnear RPL37P25 · rs1544780
See detailed info → StandardHLCS · rs13047322
See detailed info → Standardnear NFAT5 · rs12921716
See detailed info → StandardESR1 · rs9371557
See detailed info → StandardCOL27A1 · rs4978569
See detailed info → StandardHDLBP · rs3755326
See detailed info → StandardSYNJ2 · rs2502601
See detailed info → StandardRORA · rs1563565
See detailed info → Standardnear FAM76B · rs12277780
See detailed info → Standardnear BDH2P1 · rs12110525
See detailed info → StandardZNF98 · rs10414591
See detailed info → StandardPDE2A · rs1009708
See detailed info →Showing 20 of 10923 · page 151 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.