8,408 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.
KCNH2 · rs7789146
See detailed info → StandardCDK6 · rs56201652
See detailed info → StandardKDM1B · rs34969716
See detailed info → StandardSLIT3 · rs12188351
See detailed info → StandardHCN4 · rs7183206
See detailed info → StandardCAV1/2 · rs11773845
See detailed info → StandardKCNJ5 · rs75190942
See detailed info → StandardMSRA · rs17150703
See detailed info → StandardGNAT2 · rs17024258
See detailed info → StandardZZZ3 · 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 →Showing 20 of 8408 · page 414 of 421
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.