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.
PCIF1 · rs3827066
See detailed info → Sensitivenear NGF · rs11806316
See detailed info → SensitiveMAD1L1 · rs10267593
See detailed info → SensitiveCDC25A · rs7617773
See detailed info → SensitiveTSPAN14 · rs17680741
See detailed info → SensitiveHTRA1 · rs4752700
See detailed info → SensitiveKIAA1462 · rs9337951
See detailed info → SensitiveBMP1 · rs73225842
See detailed info → SensitiveTEX41 · rs7604735
See detailed info → SensitiveSEMA5A · rs17263917
See detailed info → SensitiveUHRF1BP1 · rs9469890
See detailed info → SensitiveMIR6890 · rs73082363
See detailed info → SensitiveCETP · rs56228609
See detailed info → SensitiveANKRD13B · rs7220401
See detailed info → Sensitivenear EIF2B2 · rs10131894
See detailed info → Sensitivenear STN1 · rs4918072
See detailed info → SensitivePRDM16 · rs2493298
See detailed info → SensitiveFGD5 · rs1077534
See detailed info → SensitivePALLD · rs7696431
See detailed info → SensitiveFOXC1 · rs62390615
See detailed info →Showing 20 of 256 · page 11 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.