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
10,966 positions on this site are linked to Height, out of 2,505,820 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
PDK4-AS1 · rs4379388
See detailed info → StandardTNKS2 · rs2258946
See detailed info → StandardLPAR1 · rs12552348
See detailed info → Standardnear MIR7702 · rs10980820
See detailed info → Standardnear GPAM · rs10787433
See detailed info → StandardDCTN2 · rs775241
See detailed info → StandardSTK3 · rs2922078
See detailed info → StandardCFAP65 · rs17654949
See detailed info → StandardPPP2R2A · rs17309613
See detailed info → StandardLINC02880 · rs17075678
See detailed info → StandardADAMTS17 · rs12915884
See detailed info → StandardDRAM1 · rs10860822
See detailed info → Standardnear ZBTB7C · rs1011076
See detailed info → StandardTMEM8B · rs10758328
See detailed info → StandardDEAF1 · rs7479861
See detailed info → StandardKATNBL1 · rs17817770
See detailed info → StandardNPPC · rs10460436
See detailed info → StandardANKS1A · rs144626118
See detailed info → StandardTSGA10 · rs13396584
See detailed info → Standardnear SOWAHB · rs2703115
See detailed info →Showing 20 of 10966 · page 159 of 549
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.