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
11,993 positions on this site are linked to Height, out of 2,519,740 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
NPR2 · rs2281645
See detailed info → StandardESR1 · rs9322335
See detailed info → StandardLUZP1 · rs643492
See detailed info → StandardCYBRD1 · rs3821083
See detailed info → StandardTC2N · rs759232
See detailed info → StandardFLNB · rs839239
See detailed info → StandardCHSY1 · rs8042424
See detailed info → StandardCD79B · rs8077653
See detailed info → StandardZBTB38 · rs6762722
See detailed info → Standardnear GUSBP5 · rs17017907
See detailed info → StandardLTBP1 · rs5024713
See detailed info → StandardDNM3 · rs10489286
See detailed info → StandardCDK6-AS1 · rs7793983
See detailed info → StandardFANCD2OS · rs6792811
See detailed info → StandardSKAP1 · rs41336845
See detailed info → StandardECM2 · rs4743873
See detailed info → StandardADAMTS17 · rs2035344
See detailed info → StandardTULP4 · rs705930
See detailed info → Standardnear Y_RNA · rs2902407
See detailed info → Standardnear PTCH1 · rs17370391
See detailed info →Showing 20 of 11993 · page 73 of 600
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.