12,481 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.
ZBTB5 · rs17502738
See detailed info → StandardASCL4 · rs60222088
See detailed info → StandardALG10B · rs35011311
See detailed info → StandardEMPI1 · rs2417268
See detailed info → StandardTRPC6 · rs11224896
See detailed info → StandardFADS2 · rs174541
See detailed info → StandardADO · rs224111
See detailed info → StandardTMEM38B · rs971415
See detailed info → StandardTLE4 · rs13284688
See detailed info → StandardKSR2 · rs11615756
See detailed info → SensitiveHIP1 · rs1167796
See detailed info → StandardAUTS2 · rs6943555
See detailed info → Standard on its ownRFT1 · rs13088281
See detailed info → SensitiveHNF4A · rs4812829
See detailed info → StandardANK1 · rs6474359
See detailed info → Standard on its ownCAPZB · rs12138950
See detailed info → StandardPTPN11 · rs11066301
See detailed info → SensitiveRASD1 · rs12936587
See detailed info → Standard on its ownTRPM6 · rs11144134
See detailed info → Standard on its ownSHROOM3 · rs13146355
See detailed info →Showing 20 of 12481 · page 558 of 625
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.