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
11,452 positions on this site are linked to Height, out of 2,509,139 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
BTN3A3 · rs181680390
See detailed info → Standardnear SLAIN2 · rs177956
See detailed info → StandardLRP1B · rs17516630
See detailed info → StandardTSBP1-AS1 · rs17495612
See detailed info → StandardTRAF3IP2-AS1 · rs174388
See detailed info → StandardARHGAP29-AS1 · rs17400584
See detailed info → StandardSUGT1P4-STRA6LP-CCDC180 · rs16919164
See detailed info → StandardLINC00973 · rs1607782
See detailed info → Standardnear RNA5SP45 · rs1537522
See detailed info → StandardLETM1 · rs150992198
See detailed info → StandardSLC38A6 · rs150150402
See detailed info → StandardFRMD5 · rs149779816
See detailed info → StandardMIR4290HG · rs148163688
See detailed info → StandardCCDC91 · rs146046988
See detailed info → Standardnear CTSK · rs145873050
See detailed info → StandardACP2 · rs145420520
See detailed info → StandardCARMIL1 · rs144503707
See detailed info → StandardNOX4 · rs144367743
See detailed info → Standardnear ALPL · rs143553186
See detailed info → Standardnear CHAC1 · rs142965947
See detailed info →Showing 20 of 11452 · page 241 of 573
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.