7,939 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.
near ZNF518B · rs79824542
See detailed info → SensitivePTHLH · rs10771399
See detailed info → StandardZNF518B · rs34208161
See detailed info → Standard on its ownC17orf71 · rs6503905
See detailed info → Standard on its ownMPO · rs12940923
See detailed info → StandardSLC2A9 · rs80204783
See detailed info → StandardSLC2A9 · rs116142041
See detailed info → StandardACOXL · rs17483466
See detailed info → StandardMNS1 · rs11636802
See detailed info → SensitiveCDCA7 · rs4972593
See detailed info → StandardADCY9 · rs879620
See detailed info → StandardPCSK1 · rs7713317
See detailed info → Standard on its ownADCY5 · rs11708067
See detailed info → StandardSLC22A3 · rs539958
See detailed info → StandardSTK36 · rs1427445
See detailed info → StandardCCDC92-DNAH10 · rs7133378
See detailed info → StandardINHBC · rs3741414
See detailed info → StandardARL15 · rs3776717
See detailed info → StandardETV5 · rs4234589
See detailed info → Standard on its ownSLC30A10 · rs2820443
See detailed info →Showing 20 of 7939 · page 289 of 397
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.