10 positions on this site are linked to Meniere's Disease, out of 94,714 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
LINC01088 · rs115058055
See detailed info → SensitiveCAMK1D · rs533941215
See detailed info → Sensitivenear RNU6-832P · rs979245270
See detailed info → SensitiveSLC37A3 · rs553411385
See detailed info → SensitivePRDM11 · rs149479122
See detailed info → SensitiveVPS13B · rs76416960
See detailed info → SensitiveTRABD2B · rs75323670
See detailed info → SensitiveEYA4 · rs3777811
See detailed info → SensitiveBRMS1L · rs529699157
See detailed info → Sensitivenear XRCC6P1 · rs61861121
See detailed info →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.