8,083 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.
SLIT3 · rs2163761
See detailed info → StandardCPNE8 · rs826838
See detailed info → StandardCD46 · rs11118555
See detailed info → StandardSULT1C2 · rs17770672
See detailed info → StandardCOL21A1 · rs9475677
See detailed info → StandardULK4 · rs1353394
See detailed info → StandardCD34 · rs11578508
See detailed info → StandardB3GNT7 · rs13030174
See detailed info → StandardLINC00477 · rs17287293
See detailed info → StandardFLRT2 · rs17796783
See detailed info → StandardGNG11 · rs180242
See detailed info → StandardTFPI · rs4140885
See detailed info → StandardKLHL42 · rs7133214
See detailed info → StandardMYT1L · rs4553849
See detailed info → StandardCNR1 · rs6933130
See detailed info → StandardSUCLG1 · rs2084597
See detailed info → StandardDGKG · rs35598536
See detailed info → StandardSEMA5A · rs1666789
See detailed info → StandardNUDT12 · rs76482840
See detailed info → Standard on its ownASIP · rs6059655
See detailed info →Showing 20 of 8083 · page 252 of 405
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.