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
10,966 positions on this site are linked to Height, out of 2,505,820 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
ADAMTS6 · rs967459
See detailed info → StandardSPRED1 · rs940026
See detailed info → StandardLUNAR1 · rs8037680
See detailed info → StandardSTRA8 · rs7806817
See detailed info → StandardCREB5 · rs767834
See detailed info → StandardSNAI1 · rs4647955
See detailed info → Standardnear DYNLL2 · rs181222
See detailed info → StandardSLIT3 · rs17553680
See detailed info → StandardBLTP3A · rs16894945
See detailed info → Standardnear TACC1 · rs16887815
See detailed info → Standardnear RN7SL366P · rs1555227
See detailed info → StandardTGFBR2 · rs12490466
See detailed info → Standardnear SEC16B · rs10798580
See detailed info → StandardARMC2 · rs3734651
See detailed info → StandardCDK6 · rs117796712
See detailed info → StandardFUBP3 · rs11243976
See detailed info → StandardCENPO · rs2278483
See detailed info → StandardCRTC1 · rs2240013
See detailed info → StandardEEF2 · rs2230561
See detailed info → Standardnear MTND5P40 · rs17248705
See detailed info →Showing 20 of 10966 · page 144 of 549
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.