12,425 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.
XPO7 · rs6998692
See detailed info → StandardKCNN2 · rs716845
See detailed info → StandardTHRB · rs73032363
See detailed info → StandardSLC35F1 · rs281868
See detailed info → StandardPKD2L2 · rs6864727
See detailed info → StandardCEP68 · rs2723064
See detailed info → StandardMETTL11B · rs10800507
See detailed info → StandardDMRTA2 · rs56202902
See detailed info → StandardPHLDB2 · rs73228543
See detailed info → StandardMIR30B · rs7460121
See detailed info → StandardATXN1 · rs7770062
See detailed info → StandardFBXO32 · rs78332318
See detailed info → StandardXPO7 · rs7846485
See detailed info → StandardLINC00540 · rs7987944
See detailed info → StandardLRRC74 · rs8181996
See detailed info → StandardSORL1 · rs949078
See detailed info → StandardNUCKS1 · rs951366
See detailed info → StandardRASSF8 · rs117640426
See detailed info → StandardMSRA · rs7826222
See detailed info → StandardPRRX1 · rs503706
See detailed info →Showing 20 of 12425 · page 613 of 622
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.