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
1,538 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 2,506,432 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
near C2CD2 · rs116376114
See detailed info → StandardLRRK2 · rs1907631
See detailed info → StandardCCDC170 · rs9371220
See detailed info → StandardACAD11 · rs17345563
See detailed info → StandardMYLIP · rs2294261
See detailed info → StandardLDLRAP1 · rs11802413
See detailed info → StandardLDLR · rs2738452
See detailed info → StandardST3GAL4 · rs2401
See detailed info → StandardLCAT · rs1109166
See detailed info → StandardCMTM6 · rs3773777
See detailed info → StandardFN1 · rs1250248
See detailed info → StandardFAM117B · rs6435161
See detailed info → StandardPHLDB1 · rs17122278
See detailed info → StandardERGIC3 · rs7264396
See detailed info → StandardAPOB · rs10172650
See detailed info → StandardFRK · rs868943
See detailed info → StandardLDLR · rs4804155
See detailed info → StandardTRIB1 · rs2980869
See detailed info → StandardHNF1A · rs2244608
See detailed info → StandardBLOC1S3 · rs149553138
See detailed info →Showing 20 of 1538 · page 74 of 77
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.