9,424 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.
KCNN2 · rs716845
See detailed info → StandardXPO7 · rs6998692
See detailed info → StandardPITX2 · rs6847935
See detailed info → StandardCAND2 · rs6810325
See detailed info → StandardKIF3C · rs6546620
See detailed info → StandardUSP3 · rs62011291
See detailed info → StandardGORAB · rs608930
See detailed info → StandardCAMK2D · rs55754224
See detailed info → StandardPRRX1 · rs503706
See detailed info → StandardNUCKS1 · rs4951261
See detailed info → StandardGNB4 · rs4855075
See detailed info → StandardZNF462 · rs4743034
See detailed info → StandardC9orf3 · rs4385527
See detailed info → StandardPTK2 · rs4355822
See detailed info → StandardCCDC92 · rs3789967
See detailed info → StandardBEST3 · rs35349325
See detailed info → StandardMTSS1 · rs35006907
See detailed info → StandardKCNN3 · rs34292822
See detailed info → StandardSPATS2L · rs295114
See detailed info → StandardNAV2 · rs2625322
See detailed info →Showing 20 of 9424 · page 458 of 472
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.