118,504 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.
RYR1 · rs34934920
See detailed info → StandardRYR1 · rs35648526
See detailed info → StandardRYR1 · rs113017076
See detailed info → StandardRYR1 · rs4801763
See detailed info → StandardRYR1 · rs34853245
See detailed info → StandardRYR1 · rs78341134
See detailed info → SensitiveRYR1 · rs118192172
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.