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
11,048 positions on this site are linked to Height, out of 2,506,243 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
KLHL29 · rs1991083
See detailed info → StandardCABLES1 · rs17186875
See detailed info → StandardCRADD · rs1471816
See detailed info → Standardnear C17orf67 · rs1401796
See detailed info → StandardIGF1R · rs13379905
See detailed info → Standardnear KRT18P35 · rs13072100
See detailed info → StandardDLEU1 · rs1262774
See detailed info → StandardHAGHL · rs12448432
See detailed info → Standardnear PTCH1 · rs12343296
See detailed info → Standardnear ZMIZ1 · rs11002928
See detailed info → StandardCDC14B · rs10991378
See detailed info → Standardnear AK4P2 · rs10940473
See detailed info → StandardGFPT2 · rs1035412
See detailed info → StandardITGB8 · rs10265149
See detailed info → StandardDIS3L2 · rs76803230
See detailed info → StandardZRANB3 · rs1900741
See detailed info → StandardRFC1 · rs2066789
See detailed info → StandardNEPRO-AS1 · rs1903431
See detailed info → StandardTMEM229B · rs8019974
See detailed info → StandardGNA12 · rs2266925
See detailed info →Showing 20 of 11048 · page 551 of 553
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.