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
10,920 positions on this site are linked to Height, out of 2,505,240 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
MRTFB · rs17196874
See detailed info → StandardLINC01104 · rs13026283
See detailed info → Standardnear RPL23AP75 · rs11078945
See detailed info → Standardnear CDC16 · rs7336692
See detailed info → StandardCGNL1 · rs2131740
See detailed info → Standardnear RXRG · rs17429123
See detailed info → StandardHCG27 · rs540536098
See detailed info → StandardOTUD4 · rs35856976
See detailed info → StandardLMO7 · rs17704212
See detailed info → StandardAKR1C2 · rs10904387
See detailed info → Standardnear ANKFN1 · rs10515131
See detailed info → StandardTAF5 · rs7905968
See detailed info → StandardHABP4 · rs7870753
See detailed info → StandardTTBK2 · rs7173097
See detailed info → StandardPCSK5 · rs7027130
See detailed info → StandardZFHX3 · rs328365
See detailed info → Standardnear POLR1F · rs2390151
See detailed info → StandardATXN7L1 · rs2272172
See detailed info → StandardCSMD1 · rs17071968
See detailed info → StandardVCL · rs12413620
See detailed info →Showing 20 of 10920 · page 145 of 546
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.