7,431 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.
KLHL42 · 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 → SensitiveSLC10A2 · rs16961023
See detailed info → StandardRAB38 · rs16913594
See detailed info → StandardLYZL1 · rs1889714
See detailed info → StandardLYZL1 · rs1248290
See detailed info → StandardLINGO2 · rs10969143
See detailed info → SensitiveNRG1 · rs7005606
See detailed info → StandardVANGL1 · rs12137699
See detailed info → StandardCYP2A6 · rs7247903
See detailed info → StandardCYP2G1P · rs73931391
See detailed info → StandardRAB4B-EGLN2 · rs185308415
See detailed info → StandardRAB4B-EGLN2 · rs7507400
See detailed info → StandardTSPYL5 · rs2045966
See detailed info →Showing 20 of 7431 · page 220 of 372
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.