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.
DCST2 · rs905938
See detailed info → StandardGFRA3 · rs10040989
See detailed info → StandardATP1B1 · rs545833
See detailed info → StandardNOS1AP · rs164133
See detailed info → StandardNOS1AP · rs347272
See detailed info → StandardNOS1AP · rs17460657
See detailed info → StandardNCOA2 · rs16936870
See detailed info → StandardKCNH2 · rs2072413
See detailed info → StandardCAV1 · rs9920
See detailed info → StandardSLC35F1 · rs9489510
See detailed info → StandardSLC4A4 · rs2363719
See detailed info → StandardTTN · rs7561149
See detailed info → StandardSP3 · rs938291
See detailed info → StandardATP1B1 · rs12079745
See detailed info → StandardATP1B1 · rs10919070
See detailed info → SensitiveSOX9 · rs4793529
See detailed info → StandardTCEA3 · rs2298632
See detailed info → StandardNOS1AP · rs6669543
See detailed info → StandardRNF207 · rs2273042
See detailed info → StandardNOS1AP · rs16857031
See detailed info →Showing 20 of 8790 · page 323 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.