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
11,639 positions on this site are linked to Height, out of 2,511,480 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
PHC2-AS1 · rs4652856
See detailed info → Standardnear Y_RNA · rs300904
See detailed info → StandardCCDC26 · rs2062078
See detailed info → StandardPIGPP3 · rs4012234
See detailed info → Standardnear H6PD · rs11590326
See detailed info → Standardnear MAP3K3 · rs11867396
See detailed info → StandardZFAT-AS1 · rs7004326
See detailed info → StandardCAPZB · rs1472565
See detailed info → StandardMEF2C-AS1 · rs2011071
See detailed info → StandardJAZF1 · rs508347
See detailed info → StandardPITX1-AS1 · rs39881
See detailed info → StandardECE1 · rs212526
See detailed info → Standardnear GIGYF1 · rs221784
See detailed info → StandardFGFRL1 · rs34627176
See detailed info → StandardKPNB1-DT · rs4794001
See detailed info → StandardCWC27 · rs264766
See detailed info → StandardSTAT1 · rs6718902
See detailed info → StandardZBTB20-AS5 · rs9873460
See detailed info → StandardDIPK1A · rs10874746
See detailed info → StandardHOMEZ · rs8017130
See detailed info →Showing 20 of 11639 · page 16 of 582
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.