9,424 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.
SEC16B · rs633715
See detailed info → StandardOLFM4 · rs9568867
See detailed info → StandardLINGO2 · rs10968576
See detailed info → StandardSH3PXD2A · rs10509768
See detailed info → StandardLRMDA · rs16932995
See detailed info → StandardCAV1 · rs9886216
See detailed info → StandardKCNN2 · rs1013168
See detailed info → StandardHAND2 · rs10024737
See detailed info → StandardPITX2 · rs16997168
See detailed info → StandardRASSF8 · rs117640426
See detailed info → StandardNUCKS1 · rs951366
See detailed info → StandardSORL1 · rs949078
See detailed info → StandardLRRC74 · rs8181996
See detailed info → StandardLINC00540 · rs7987944
See detailed info → StandardXPO7 · rs7846485
See detailed info → StandardFBXO32 · rs78332318
See detailed info → StandardATXN1 · rs7770062
See detailed info → StandardMIR30B · rs7460121
See detailed info → StandardPHLDB2 · rs73228543
See detailed info → StandardTHRB · rs73032363
See detailed info →Showing 20 of 9424 · page 457 of 472
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.