256 positions on this site are linked to Coronary Artery Disease, out of 107,180 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near IGF2R · rs6932293
See detailed info → SensitiveWDR12 · rs148812085
See detailed info → SensitivePHACTR1 · rs9381634
See detailed info → SensitiveHSD17B12 · rs7116641
See detailed info → SensitivePARP12 · rs2269997
See detailed info → SensitiveFN1 · rs17517928
See detailed info → SensitiveASAP2 · rs2715879
See detailed info → SensitiveATP1B3 · rs7622417
See detailed info → Sensitivenear CRTAC1 · rs1867073
See detailed info → Sensitivenear RNU6-1064P · rs944172
See detailed info → SensitiveHHIPL1 · rs12893887
See detailed info → SensitiveACSM5 · rs9929808
See detailed info → SensitiveCDKN2B-AS1 · rs6475608
See detailed info → SensitiveCTSS · rs6587520
See detailed info → Sensitivenear CDC123 · rs61848342
See detailed info → SensitiveRAB3GAP1 · rs6730157
See detailed info → SensitivePCSK9 · rs45448095
See detailed info → SensitiveCUX2 · rs3858704
See detailed info → Sensitivenear LINC03089 · rs494207
See detailed info → SensitivePPAP2B · rs17114046
See detailed info →Showing 20 of 256 · page 6 of 13
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.