12,423 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.
LOC84931 · rs2030746
See detailed info → StandardVLDLR · rs3780181
See detailed info → StandardPIGV · rs12748152
See detailed info → StandardNYNRIN · rs8017377
See detailed info → StandardINSIG2 · rs10490626
See detailed info → Standard on its ownFILIP1L · rs9811920
See detailed info → StandardSNTB1 · rs6469937
See detailed info → Standard on its ownSCN5A · rs1805126
See detailed info → Standard on its ownARHGAP18 · rs12193446
See detailed info → StandardFILIP1L · rs13081855
See detailed info → StandardKLK2 · rs1354774
See detailed info → StandardMPP1 · rs5987027
See detailed info → SensitiveSLC17A8 · rs12296850
See detailed info → StandardAlpha-globin cluster · rs7203560
See detailed info → Standard on its ownHTR1A · rs7445832
See detailed info → StandardDARC · rs4657616
See detailed info → StandardSOX9 · rs11654749
See detailed info → StandardKCNE1 · rs1805128
See detailed info → StandardLIG3 · rs1052536
See detailed info → StandardCOLEC10 · rs2450083
See detailed info →Showing 20 of 12423 · page 529 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.