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 2,505,145 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
DENND6A · rs4681651
See detailed info → StandardACY3 · rs2514037
See detailed info → StandardLINC00629 · rs2503987
See detailed info → Standardnear AHCYP3 · rs13389563
See detailed info → StandardDNM2 · rs12459870
See detailed info → StandardSEPTIN9 · rs11655686
See detailed info → Standardnear KRT18P51 · rs76390704
See detailed info → StandardDYSF · rs6739650
See detailed info → StandardCPNE7 · rs34395984
See detailed info → StandardAIFM1 · rs209999
See detailed info → StandardTHSD4 · rs17737516
See detailed info → StandardHDAC9 · rs17140133
See detailed info → Standardnear SLC9A9 · rs9839394
See detailed info → StandardCOL11A2 · rs9469378
See detailed info → StandardERC1 · rs7973282
See detailed info → StandardRUVBL2 · rs7256033
See detailed info → StandardPTPRN · rs6736979
See detailed info → Standardnear PDCD2 · rs4428484
See detailed info → Standardnear ATE1 · rs17544933
See detailed info → StandardDDX19B · rs16970606
See detailed info →Showing 20 of 10920 · page 142 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.