8,605 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.
H6PD · rs6662509
See detailed info → StandardAMZ1 · rs798554
See detailed info → SensitiveC1QBP · rs72634030
See detailed info → SensitiveATG5 · rs9372120
See detailed info → SensitiveC4orf52 · rs11933540
See detailed info → SensitiveCD226 · rs2469434
See detailed info → SensitiveARID5B · rs71508903
See detailed info → SensitiveC5orf30 · rs2561477
See detailed info → SensitiveCCL19 · rs11574914
See detailed info → SensitiveAFF3 · rs9653442
See detailed info → StandardPOMC · rs1561288
See detailed info → StandardSHANK3 · rs6010044
See detailed info → SensitiveCACNA1C · rs1006737
See detailed info → SensitiveNSUN6 · rs17691888
See detailed info → SensitiveGRIA1 · rs17504622
See detailed info → SensitiveGIGYF2 · rs778371
See detailed info → SensitiveMMP16 · rs11995572
See detailed info → SensitiveZSWIM6 · rs171748
See detailed info → StandardDIP2B · rs7968440
See detailed info → StandardLEPR · rs1938492
See detailed info →Showing 20 of 8605 · page 340 of 431
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.