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 2,506,722 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
ASAH2B · rs71489325
See detailed info → Standardnear SOD1 · rs73349629
See detailed info → StandardSLC19A1 · rs73907602
See detailed info → StandardOSBP · rs12276505
See detailed info → StandardZGPAT · rs62217799
See detailed info → Standardnear FIZ1 · rs12610709
See detailed info → StandardCNPY3 · rs1053539
See detailed info → StandardPATL1 · rs11230036
See detailed info → StandardCCDC12 · rs13092573
See detailed info → StandardPAQR6 · rs2075165
See detailed info → StandardRCOR1 · rs4900550
See detailed info → StandardMAST3 · rs67234314
See detailed info → Standardnear ADRB1 · rs72823014
See detailed info → StandardABCA9 · rs76263023
See detailed info → StandardBMAL1 · rs6486121
See detailed info → StandardVMP1 · rs2453913
See detailed info → StandardSLC30A10 · rs61836039
See detailed info → StandardCHLSN · rs12702029
See detailed info → StandardAHSG · rs2070635
See detailed info → StandardCAMK2B · rs62459087
See detailed info →Showing 20 of 1538 · page 68 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.