24 positions on this site are linked to Hypertrophic Cardiomyopathy, out of 98,410 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
LINC02775 · rs74139614
See detailed info → StandardSTRN · rs7588378
See detailed info → StandardAC103855.3 · rs74605438
See detailed info → StandardHLF · rs17817857
See detailed info → Standardnear LSM3 · rs13061705
See detailed info → StandardOR5AK2 · rs139913353
See detailed info → Standardnear MS4A6E · rs185502387
See detailed info → Standardnear TBX3-AS1 · rs7487962
See detailed info → StandardAMBRA1 · rs142929136
See detailed info → Standardnear OR5B12 · rs546759453
See detailed info → StandardFHOD3 · rs4799426
See detailed info → StandardARHGAP1 · rs187474069
See detailed info → StandardPRG3 · rs764568652
See detailed info → StandardTMEM182 · rs2540277
See detailed info → StandardTRDN-AS1 · rs9320939
See detailed info → StandardSYNPO2L · rs3740293
See detailed info → StandardFHOD3 · rs118060942
See detailed info → Standardnear OR5BQ1P · rs78310129
See detailed info → StandardPRKCA · rs7210446
See detailed info → StandardDNAJC18 · rs4385202
See detailed info →Showing 20 of 24 · page 1 of 2
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.