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
10,753 positions on this site are linked to Height, out of 2,500,639 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 RPSAP72 · rs682310
See detailed info → StandardPPP2R5E · rs6573522
See detailed info → Standardnear LINC01982 · rs6504769
See detailed info → Standardnear LINC01664 · rs5994170
See detailed info → StandardLINC01868 · rs4851365
See detailed info → StandardLMNB1 · rs3749830
See detailed info → StandardSLC31A2 · rs2571
See detailed info → StandardKALRN · rs11714061
See detailed info → StandardSAMD13 · rs1156085
See detailed info → StandardSLC4A4 · rs1134115
See detailed info → StandardTMTC2 · rs11115413
See detailed info → StandardADAMTS6 · rs967459
See detailed info → StandardSPRED1 · rs940026
See detailed info → StandardLUNAR1 · rs8037680
See detailed info → StandardSTRA8 · rs7806817
See detailed info → StandardCREB5 · rs767834
See detailed info → StandardSNAI1 · rs4647955
See detailed info → Standardnear DYNLL2 · rs181222
See detailed info → StandardSLIT3 · rs17553680
See detailed info → StandardBLTP3A · rs16894945
See detailed info →Showing 20 of 10753 · page 140 of 538
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.