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.
GOSR2 · rs17608766
See detailed info → StandardKLF12 · rs1886512
See detailed info → Standardnear LEKR1 · rs900399
See detailed info → StandardHNF1A · rs1183910
See detailed info → StandardPTPN2 · rs1893217
See detailed info → Sensitivenear PMCH · rs76770509
See detailed info → Standardnear CTIF · rs7240004
See detailed info → StandardNOTCH1 · rs13300218
See detailed info → Standardnear FAP · rs2111485
See detailed info → StandardIRF1 · rs17622378
See detailed info → StandardSLC39A11 · rs17780256
See detailed info → Standardnear TRAF3IP2 · rs3851228
See detailed info → StandardNR5A2 · rs2816958
See detailed info → Standardnear IFNG · rs7134472
See detailed info → Standardnear KIR3DL2 · rs17771967
See detailed info → StandardCYTH1 · rs17736589
See detailed info → StandardBLTP1 · rs7657746
See detailed info → StandardLITAF · rs11641184
See detailed info → Standardnear SLC39A11 · rs7210086
See detailed info → Standardnear USP12 · rs17085007
See detailed info →Showing 20 of 12444 · page 601 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.