12,444 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.
ACE · rs4343
See detailed info → StandardRGS11 · rs2858942
See detailed info → Standard on its ownTYR · rs1042602
See detailed info → Standard on its ownFUT2 · rs2287921
See detailed info → SensitiveLSP1 · rs3817198
See detailed info → SensitiveLDLR · rs1122608
See detailed info → StandardSLC18A1 · rs326
See detailed info → SensitiveNOTCH2 · rs10923931
See detailed info → SensitiveANK3 · rs10994336
See detailed info → StandardSLC2A9 · rs16890979
See detailed info → StandardGSDMC · rs987525
See detailed info → StandardRCL1 · rs2236496
See detailed info → Standard on its ownCASR · rs17251221
See detailed info → StandardSLC2A9 · rs13129697
See detailed info → StandardTERC · rs12696304
See detailed info → SensitiveNCAN · rs1064395
See detailed info → SensitivePRKCI · rs71277158
See detailed info → SensitiveLOC338694 · rs7929962
See detailed info → SensitiveRASA1 · rs35148638
See detailed info → Sensitivenear POU5F1B · rs16901979
See detailed info →Showing 20 of 12444 · page 590 of 623
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.