8,790 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.
ABCC11 · rs17822931
See detailed info → StandardSLC45A2 · rs16891982
See detailed info → StandardHERC2 / OCA2 · rs12913832
See detailed info → StandardADH1B · rs1229984
See detailed info → StandardCYP1A2 · rs762551
See detailed info → StandardMCM6 / LCT · rs4988235
See detailed info → SensitiveF5 · rs6025
See detailed info → StandardMTHFR · rs1801133
See detailed info → StandardOPRM1 · rs1799971
See detailed info → SensitiveAPOE · rs429358-rs7412
See detailed info →Showing 10 of 8790 · page 440 of 440
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.