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
10,923 positions on this site are linked to Height, out of 2,505,333 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
FOXP2 · rs1868757
See detailed info → StandardPTPN13 · rs17454077
See detailed info → StandardCERK · rs12628356
See detailed info → StandardLINC02732 · rs11213366
See detailed info → StandardSLC52A1 · rs346823
See detailed info → Standardnear CD180 · rs16896422
See detailed info → StandardADAMTSL1 · rs17801409
See detailed info → StandardPRXL2A · rs17617406
See detailed info → Standardnear RGMA · rs10520714
See detailed info → StandardDHCR24 · rs6676123
See detailed info → Standardnear EXOSC8P1 · rs2782256
See detailed info → StandardPBRM1 · rs1992193
See detailed info → StandardSCAND3 · rs114904171
See detailed info → StandardCCDC88A · rs6746287
See detailed info → StandardMIRLET7BHG · rs16994846
See detailed info → StandardFAM13A · rs1343921
See detailed info → StandardZNF678 · rs10916167
See detailed info → StandardST3GAL1 · rs7820431
See detailed info → StandardTSPAN33 · rs11767848
See detailed info → StandardENTPD7 · rs11596177
See detailed info →Showing 20 of 10923 · page 150 of 547
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.