10,913 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.
CCDC92 · rs4765127
See detailed info → SensitiveAPOB · rs10199768
See detailed info → StandardHNF1A · rs2393791
See detailed info → StandardCOBLL1 · rs10195252
See detailed info → Sensitivenear ZNF518B · rs4698036
See detailed info → SensitiveBCHE · rs1803274
See detailed info → SensitiveLPL · rs17091905
See detailed info → StandardNAT2 · rs1495741
See detailed info → StandardBANK1 · rs6846071
See detailed info → Standard on its ownSC4MOL · rs17046216
See detailed info → Standard on its ownTCERG1L · rs10829848
See detailed info → StandardADAMTS-8 · rs11222084
See detailed info → StandardNOV · rs2071518
See detailed info → SensitivePLCE1 · rs2274223
See detailed info → Standard on its ownPCSK1 · rs6235
See detailed info → StandardITPA · rs6139030
See detailed info → SensitiveANP32A · rs8030672
See detailed info → Standard on its ownLARP6 · rs1549318
See detailed info → Standard on its ownSLC30A8 · rs11558471
See detailed info → StandardNAT8 · rs9309473
See detailed info →Showing 20 of 10913 · page 493 of 546
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.