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
11,375 positions on this site are linked to Height, out of 2,508,576 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
near BSX · rs10892940
See detailed info → StandardDDX23 · rs1057908
See detailed info → Standardnear MIR375 · rs371825
See detailed info → Standardnear RPL23AP75 · rs1009570
See detailed info → StandardLNCAROD · rs6480933
See detailed info → Standardnear RPS4XP9 · rs9375460
See detailed info → StandardMED13L · rs10507271
See detailed info → StandardDIRC3 · rs4672846
See detailed info → StandardRPS10-NUDT3 · rs206930
See detailed info → StandardRSPO2 · rs555008
See detailed info → Standardnear ZCCHC24 · rs1923367
See detailed info → StandardEIF2AK3 · rs1913671
See detailed info → StandardPDE8B · rs4704397
See detailed info → Standardnear OPN4 · rs2250515
See detailed info → StandardFGF18 · rs6887323
See detailed info →Showing 15 of 11375 · page 569 of 569
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.