103,022 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.
NOS1AP · rs164133
See detailed info → StandardNOS1AP · rs347272
See detailed info → StandardNOS1AP · rs16857031
See detailed info → StandardNOS1AP · rs17457880
See detailed info → StandardNOS1AP · rs6669543
See detailed info → StandardNOS1AP · rs73017364
See detailed info → StandardNOS1AP · rs12567315
See detailed info → StandardNOS1AP · rs12029454
See detailed info →Showing 8 of 28 · page 2 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.