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
11,181 positions on this site are linked to Height, out of 2,507,049 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
ZNF638 · rs7568069
See detailed info → StandardPRKCA · rs72843895
See detailed info → StandardPOGZ · rs72710154
See detailed info → StandardSTRADA · rs187182984
See detailed info → StandardDNM3 · rs12410416
See detailed info → Standardnear DAAM2 · rs12215132
See detailed info → StandardKCNJ15 · rs9983533
See detailed info → StandardFOXP1 · rs80190719
See detailed info → Standardnear PRSS38 · rs74140388
See detailed info → Standardnear LINC00681 · rs4510865
See detailed info → StandardSMAD7 · rs3764482
See detailed info → Standardnear ZNF322 · rs371116791
See detailed info → StandardPIEZO1 · rs2926774
See detailed info → StandardACAN · rs146576224
See detailed info → StandardDNMT3A · rs141473447
See detailed info → StandardIGF1R · rs12907693
See detailed info → StandardHIVEP2 · rs12154082
See detailed info → StandardGNPTAB · rs117466029
See detailed info → StandardSLC38A4 · rs7963364
See detailed info → StandardNMRAL2P · rs57350994
See detailed info →Showing 20 of 11181 · page 526 of 560
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.