7,519 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.
ZZZ3 · rs17381664
See detailed info → StandardMRPS33P4 · rs13041126
See detailed info → StandardGAS8 · rs74583214
See detailed info → StandardCMKLR2 · rs114670539
See detailed info → StandardTNNI3K · rs10493544
See detailed info → StandardADCY3 · rs4077678
See detailed info → Standardnear MC4R · rs6567160
See detailed info → StandardTDH · rs2060457
See detailed info → StandardTBX5-AS1 · rs12810346
See detailed info → StandardLYPLAL1 · rs2605100
See detailed info → StandardMSRA · rs7826222
See detailed info → StandardTFAP2B · rs987237
See detailed info → StandardKCNMA1 · rs2116830
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 → StandardGIPR · rs10423928
See detailed info → StandardZHFX3 · rs4404097
See detailed info →Showing 20 of 7519 · page 370 of 376
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.