55 positions on this site are linked to Heart Failure, out of 24,083 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near PITX2 · rs59788391
See detailed info → StandardFTO · rs7188250
See detailed info → StandardPNMT · rs3764351
See detailed info → StandardMAP3K7CL · rs73193820
See detailed info → StandardCARM1 · rs1541596
See detailed info → Standardnear ZBTB17 · rs3961710
See detailed info → StandardNFIA · rs2474370
See detailed info → Standardnear DPT · rs114687274
See detailed info → StandardCRIM1 · rs68111949
See detailed info → StandardABCG8 · rs4076834
See detailed info → StandardSPATS2L · rs74853338
See detailed info → Standardnear CD28 · rs16840016
See detailed info → Standardnear PITX2 · rs4833443
See detailed info → Standardnear PITX2 · rs7680240
See detailed info → StandardCAMK2D · rs17620390
See detailed info → StandardPAIP2 · rs113408838
See detailed info → Standardnear NR3C1 · rs72804738
See detailed info → Standardnear ZNF318 · rs9472040
See detailed info → StandardCDK6 · rs2282979
See detailed info → StandardFLNC · rs73238153
See detailed info →Showing 20 of 55 · page 2 of 3
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.