12,426 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.
PPARD/FANCE · rs6457821
See detailed info → StandardHEYL · rs3916164
See detailed info → StandardGDF5 · rs143384
See detailed info → Standard on its ownPDE4D · rs17382202
See detailed info → StandardBCL11A · rs243070
See detailed info → StandardPRKCE · rs4953318
See detailed info → StandardACAN · rs16942341
See detailed info → StandardMSL2L1 · rs645040
See detailed info → Standard on its ownCTNNA3 · rs12251332
See detailed info → Standard on its ownABO · rs8176693
See detailed info → StandardCREB5 · rs56388170
See detailed info → StandardFAM46A · rs171835
See detailed info → Standardnear PRL · rs1205896
See detailed info → Standard on its ownASAP1 · rs4733781
See detailed info → StandardCANX · rs6893300
See detailed info → Standardnear BMP2K · rs7439923
See detailed info → StandardAFF1 · rs56390363
See detailed info → Standardnear RPN1 · rs6782812
See detailed info → StandardENSG00000225421 · rs1356493
See detailed info → StandardLINC01122 · rs2708146
See detailed info →Showing 20 of 12426 · page 537 of 622
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.