7,431 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.
SCN10A · rs6790396
See detailed info → StandardCAND2 · rs7650482
See detailed info → StandardERBB4 · rs35544454
See detailed info → StandardSPATS2L · rs3820888
See detailed info → StandardGYPC · rs28387148
See detailed info → StandardUSP34 · rs11125871
See detailed info → StandardKIF3C · rs7578393
See detailed info → StandardHAND2 · rs4615152
See detailed info → StandardNEURL1 · rs11598047
See detailed info → StandardPRRX1 · rs577676
See detailed info → StandardKCNN3 · rs36004974
See detailed info → StandardPKP2 · rs1454934
See detailed info → StandardNEURL1 · rs60848348
See detailed info → StandardNEURL1 · rs60572254
See detailed info → StandardNEBL · rs2296610
See detailed info → StandardSLC1A4 · rs2540953
See detailed info → StandardPITX2 · rs3853445
See detailed info → StandardHAND2 · rs17059534
See detailed info → StandardHCN4 · rs7164883
See detailed info → StandardSYNPO2L · rs10824026
See detailed info →Showing 20 of 7431 · page 363 of 372
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.