9,513 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.
PRSS16 · rs3800307
See detailed info → Standardnear RPS6KA4 · rs77085155
See detailed info → StandardINHBC · rs2229357
See detailed info → StandardMLXIP · rs28548845
See detailed info → StandardIDH2 · rs28508560
See detailed info → StandardABCG2 · rs2728125
See detailed info → StandardSLC22A11 · rs76741582
See detailed info → StandardNAA25 · rs116873087
See detailed info → StandardPIBF1 · rs76499759
See detailed info → StandardSLC22A11 · rs145954970
See detailed info → StandardPPM1K-DT · rs1545207
See detailed info → StandardSLC28A3 · rs548944057
See detailed info → StandardPPM1K-DT · rs28793136
See detailed info → StandardSLC17A1 · rs2817188
See detailed info → StandardWDR1 · rs75341455
See detailed info → StandardAP5B1 · rs11227299
See detailed info → StandardCHD7 · rs35914442
See detailed info → Standard on its ownHTR4 · rs7715901
See detailed info → Standard on its ownKANSL1 · rs35524223
See detailed info → Standard on its ownZKSCAN3 · rs34864796
See detailed info →Showing 20 of 9513 · page 224 of 476
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.