55 positions on this site are linked to Heart Failure, out of 23,915 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SYNPO2L · rs2177843
See detailed info → StandardELL · rs78030362
See detailed info → StandardSPRED2 · rs76704104
See detailed info → StandardTTN · rs1484116
See detailed info → StandardCAND2 · rs2305398
See detailed info → StandardSMARCB1 · rs2267039
See detailed info → Standardnear CDKN1A · rs4711456
See detailed info → StandardBRAP · rs11066001
See detailed info → StandardAOPEP · rs147288039
See detailed info → Standardnear BAZ1A · rs1712355
See detailed info → StandardUSP36 · rs6501249
See detailed info → Standardnear PMAIP1 · rs7234864
See detailed info → Standardnear FLNC · rs3807133
See detailed info → Standardnear ZNF572 · rs28455756
See detailed info → StandardMYBPC3 · rs11570058
See detailed info → StandardMLF1 · rs9864508
See detailed info → StandardPDE3A · rs7962871
See detailed info → StandardPROB1 · rs11748963
See detailed info → StandardFLNC · rs62479625
See detailed info → StandardNFIA · rs2261787
See detailed info →Showing 20 of 55 · page 1 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.