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
11,679 positions on this site are linked to Height, out of 2,512,183 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 RPSAP20 · rs1331862
See detailed info → StandardRFLNA · rs11057574
See detailed info → StandardPLA2G6 · rs6001027
See detailed info → StandardANKS1A · rs6913108
See detailed info → Standardnear LINC02817 · rs12125058
See detailed info → StandardSFRP4 · rs1721400
See detailed info → StandardMTREX · rs230755
See detailed info → StandardIP6K3 · rs652049
See detailed info → StandardFAM184B · rs2215266
See detailed info → StandardSCAND3 · rs9501180
See detailed info → StandardPSMD4 · rs16833107
See detailed info → Standardnear GPIHBP1 · rs7011172
See detailed info → Standardnear LINC02919 · rs1319584
See detailed info → StandardMTOR · rs2076655
See detailed info → StandardGMDS · rs11965306
See detailed info → StandardPSORS1C1 · rs6929464
See detailed info → StandardADAMTS17 · rs8024690
See detailed info → StandardLINC00881 · rs1403108
See detailed info → StandardNUSAP1 · rs8037574
See detailed info → StandardZNF367 · rs12002084
See detailed info →Showing 20 of 11679 · page 58 of 584
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.