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
11,879 positions on this site are linked to Height, out of 2,516,054 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
BCKDHB · rs627240
See detailed info → StandardPHF20 · rs6121073
See detailed info → StandardEDEM2 · rs6088727
See detailed info → StandardPHF20 · rs6058363
See detailed info → StandardDYM · rs549201
See detailed info → StandardESR1 · rs532010
See detailed info → StandardUQCC1 · rs4911495
See detailed info → Standardnear ADAMTS3 · rs4694508
See detailed info → Standardnear RNU2-36P · rs466390
See detailed info → StandardADAMTSL3 · rs4572348
See detailed info → StandardFGFR4 · rs434434
See detailed info → StandardDYM-AS1 · rs357909
See detailed info → StandardABCE1 · rs34149094
See detailed info → StandardANKS1A · rs2820237
See detailed info → StandardTET2-AS1 · rs2726490
See detailed info → StandardDIS3L2 · rs2633266
See detailed info → StandardETV6 · rs2187641
See detailed info → StandardDLEU1 · rs2066647
See detailed info → StandardSLFNL1 · rs17357905
See detailed info → Standardnear SUPT3H · rs16872574
See detailed info →Showing 20 of 11879 · page 63 of 594
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.