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 2,505,333 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
CD2AP · rs9369714
See detailed info → Standardnear DYNLRB2-AS1 · rs4439776
See detailed info → StandardKIAA1217 · rs7070056
See detailed info → StandardINTS2 · rs8081917
See detailed info → StandardPPM1H · rs7302602
See detailed info → Standardnear LINC02852 · rs1375227
See detailed info → StandardZBTB7C · rs10460075
See detailed info → StandardLINC03005 · rs9356834
See detailed info → StandardCNIH3 · rs7542507
See detailed info → StandardSLC7A8 · rs7157021
See detailed info → StandardZNF618 · rs3827675
See detailed info → Standardnear RPSAP72 · rs28635498
See detailed info → StandardDPY19L1 · rs17204148
See detailed info → StandardIQSEC1 · rs17037462
See detailed info → StandardLTBP1 · rs13427209
See detailed info → StandardLINC00970 · rs12048750
See detailed info → StandardPPARD · rs9296154
See detailed info → StandardDCHS1 · rs7111291
See detailed info → StandardC1QTNF7-AS1 · rs2247831
See detailed info → StandardFBN1 · rs16960943
See detailed info →Showing 20 of 10923 · page 148 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.