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.
LINC00540 · rs7987944
See detailed info → StandardXPO7 · rs7846485
See detailed info → StandardFBXO32 · rs78332318
See detailed info → StandardATXN1 · rs7770062
See detailed info → StandardMIR30B · rs7460121
See detailed info → StandardPHLDB2 · rs73228543
See detailed info → StandardTHRB · rs73032363
See detailed info → StandardKCNN2 · 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 →Showing 20 of 7431 · page 358 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.