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
11,272 positions on this site are linked to Height, out of 2,507,647 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
TRIM6-TRIM34 · rs3751006
See detailed info → Standardnear TRIP11 · rs67015182
See detailed info → StandardEGR3-AS1 · rs2313167
See detailed info → StandardANKRD52 · rs72648137
See detailed info → StandardFLI1 · rs612282
See detailed info → StandardCASC20 · rs6117293
See detailed info → Standardnear MIR548A1HG · rs17629312
See detailed info → StandardHHIP · rs1355601
See detailed info → StandardLHPP · rs10794146
See detailed info → StandardLY75 · rs2042772
See detailed info → StandardSMG6 · rs1885987
See detailed info → StandardUSP34 · rs778160
See detailed info → StandardDLEU1 · rs9535499
See detailed info → StandardPRR16 · rs1404300
See detailed info → StandardMKLN1 · rs10954312
See detailed info → StandardPDE10A · rs221730
See detailed info → StandardFNDC3B · rs1039027
See detailed info → StandardCDKN2B-AS1 · rs944802
See detailed info → Standardnear U3 · rs916893
See detailed info → StandardCYP19A1 · rs2445761
See detailed info →Showing 20 of 11272 · page 562 of 564
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.