8,005 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.
CDSN · rs111782145
See detailed info → Standard on its ownPCSK1 · rs13179048
See detailed info → Standard on its ownDPYSL5 · rs1371614
See detailed info → Standard on its ownMADD · rs7944584
See detailed info → Standard on its ownCRY2 · rs11605924
See detailed info → Standard on its ownFOXA2 · rs6048205
See detailed info → Standard on its ownSLC17A1 · rs10498730
See detailed info → Standard on its ownCASC15 · rs67258057
See detailed info → Standard on its ownSTMND1 · rs72829841
See detailed info → Standard on its ownENSG00000217379 · rs72828517
See detailed info → Standard on its ownENSG00000242753 · rs620729
See detailed info → StandardMICB · rs2596464
See detailed info → StandardIL1RL1 · rs1420101
See detailed info → StandardERBB2 · rs2952156
See detailed info → StandardMICB · rs2855812
See detailed info → StandardCLEC16A · rs17806299
See detailed info → StandardSTAT6 · rs167769
See detailed info → StandardIL1Rl1 · rs4988958
See detailed info → StandardZNF652 · rs17637472
See detailed info → Standardnear WNT16 · rs10242100
See detailed info →Showing 20 of 8005 · page 32 of 401
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.