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
11,645 positions on this site are linked to Height, out of 2,511,803 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 LINC01808 · rs11886734
See detailed info → StandardPOLR1HASP · rs3823375
See detailed info → StandardPRDM16 · rs17822581
See detailed info → StandardDAAM1 · rs10483713
See detailed info → Standardnear PCSK5 · rs7030848
See detailed info → StandardLINC01937 · rs10929290
See detailed info → StandardLPP · rs938416
See detailed info → Standardnear BMF · rs8023845
See detailed info → StandardPRKG2 · rs2868140
See detailed info → StandardAGRN · rs2710888
See detailed info → StandardMIR4713HG · rs936308
See detailed info → StandardPCGF5 · rs7069106
See detailed info → StandardBNC2 · rs10511625
See detailed info → StandardPTGR2 · rs17782239
See detailed info → StandardLINC01505 · rs9942977
See detailed info → StandardYIF1A · rs11544832
See detailed info → StandardTESHL · rs1179732
See detailed info → Standardnear CDC5L · rs3997520
See detailed info → StandardGRM4 · rs2229900
See detailed info → StandardTXNDC5 · rs9502656
See detailed info →Showing 20 of 11645 · page 33 of 583
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.