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
11,645 positions on this site are linked to Height, out of 2,511,803 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
MFSD14B · rs9409547
See detailed info → StandardLINC02664 · rs1771637
See detailed info → Standardnear LINC02919 · rs9484607
See detailed info → StandardCALU · rs6954433
See detailed info → StandardRSF1 · rs567814
See detailed info → StandardMMAB · rs11836136
See detailed info → StandardQSOX2 · rs11103398
See detailed info → Standardnear ISL1 · rs7709134
See detailed info → Standardnear TPX2 · rs6089075
See detailed info → StandardPATJ · rs2666504
See detailed info → StandardHSDL2 · rs7852741
See detailed info → StandardPDE3A · rs12318442
See detailed info → Standardnear SERPINE1 · rs757716
See detailed info → StandardLHFPL2 · rs2362831
See detailed info → Standardnear MYEOV · rs4326824
See detailed info → StandardATF7 · rs1485395
See detailed info → StandardFER1L5 · rs13014679
See detailed info → StandardDLK1 · rs117182230
See detailed info → StandardPRDM16 · rs5024246
See detailed info → StandardNOC3L · rs17439123
See detailed info →Showing 20 of 11645 · page 34 of 583
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.