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
10,923 positions on this site are linked to Height, out of 2,505,381 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 RN7SL714P · rs8022455
See detailed info → StandardNR4A3 · rs7023690
See detailed info → StandardITGA9-AS1 · rs6808722
See detailed info → StandardUBE2G2 · rs4239838
See detailed info → StandardJUN-DT · rs3015321
See detailed info → StandardPCBP1-AS1 · rs2861357
See detailed info → StandardUST · rs2333863
See detailed info → Standardnear LINC02061 · rs16889987
See detailed info → Standardnear NOG · rs12939240
See detailed info → StandardNUDT2 · rs11788425
See detailed info → Standardnear WWOX · rs11150145
See detailed info → StandardANAPC5 · rs11065547
See detailed info → StandardSASH1 · rs17715583
See detailed info → StandardANKRD44 · rs16863455
See detailed info → StandardASCC2 · rs1071962
See detailed info → StandardSNX32 · rs34924158
See detailed info → StandardCYP46A1 · rs12894973
See detailed info → StandardPLB1 · rs11679568
See detailed info → StandardRBMS3 · rs11129330
See detailed info → Standardnear TMED7 · rs6882921
See detailed info →Showing 20 of 10923 · page 152 of 547
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.