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
11,037 positions on this site are linked to Height, out of 2,506,059 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
NXNL2 · rs12685193
See detailed info → StandardCMIP · rs12149827
See detailed info → Standardnear PIEZO1P2 · rs878049
See detailed info → StandardHNRNPC · rs8016099
See detailed info → StandardLINC01606 · rs6997668
See detailed info → Standardnear CCDC91 · rs526490
See detailed info → StandardSHKBP1 · rs392726
See detailed info → StandardHCG18 · rs28780093
See detailed info → StandardTMEM39A · rs13078312
See detailed info → Standardnear REST · rs12510703
See detailed info → StandardADAM12 · rs9783128
See detailed info → StandardESR1 · rs2982554
See detailed info → StandardIPMK · rs2790232
See detailed info → StandardLINC01080 · rs1215465
See detailed info → StandardSLCO1B3-SLCO1B7 · rs11045631
See detailed info → Standardnear LINC02120 · rs1876658
See detailed info → StandardERC1 · rs7972526
See detailed info → StandardSTX8 · rs17741292
See detailed info → StandardSLC22A3 · rs609562
See detailed info → Standardnear SRFBP1 · rs9637910
See detailed info →Showing 20 of 11037 · page 174 of 552
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.