12,469 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.
TERT · rs401681
See detailed info → StandardC4 · rs2857009
See detailed info → StandardTMEM57 · rs10903129
See detailed info → Standard on its ownESR1 · rs1038304
See detailed info → StandardTRIM58 · rs11204538
See detailed info → StandardALDH7A1 · rs13182402
See detailed info → StandardC12orf67 · rs11047543
See detailed info → SensitiveHLA region · rs3131379
See detailed info → Standard on its ownBCO2 · rs2115763
See detailed info → StandardNPPA · rs17367504
See detailed info → StandardUGT1A1 · rs887829
See detailed info → Standard on its ownLASS4 · rs7258249
See detailed info → SensitiveCDKN2A · rs1011970
See detailed info → StandardPHB · rs16948048
See detailed info → Standard on its ownBRSK1 · rs1172822
See detailed info → StandardWDR66 · rs7961894
See detailed info → StandardGRAMD1B · rs735665
See detailed info → StandardMEF2D · rs3790455
See detailed info → StandardCLEC16A · rs12924729
See detailed info → StandardDIS3L2 · rs7571816
See detailed info →Showing 20 of 12469 · page 586 of 624
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.