102,854 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 · rs80159981
See detailed info → StandardNOS1AP · rs78344479
See detailed info → StandardNOS1AP · rs4657158
See detailed info → StandardNOS1AP · rs10918790
See detailed info → StandardNOS1AP · rs6684278
See detailed info → StandardNOS1AP · rs7536043
See detailed info → StandardNOS1AP · rs146009967
See detailed info → StandardNOS1AP · rs560123160
See detailed info → StandardNOS1AP · rs114836703
See detailed info → StandardNOS1AP · rs10918705
See detailed info → Standard on its ownnear NOS1AP · rs12136975
See detailed info → StandardNOS1AP · rs189676321
See detailed info → StandardNOS1AP · rs7539084
See detailed info → StandardNOS1AP · rs191648462
See detailed info → StandardNOS1AP · rs10800384
See detailed info → StandardNOS1AP · rs60441301
See detailed info → StandardNOS1AP · rs6677530
See detailed info → StandardNOS1AP · rs6658646
See detailed info → StandardNOS1AP · rs347313
See detailed info → StandardNOS1AP · rs164133
See detailed info →Showing 20 of 28 · 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.