9,061 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.
MTHFR · rs13306556
See detailed info → StandardZNF831 · rs73306888
See detailed info → StandardMSRA · rs34919878
See detailed info → StandardMECOM · rs988397
See detailed info → StandardATP2B1 · rs73437358
See detailed info → StandardPINX1 · rs4551304
See detailed info → StandardLOC105369889 · rs145485557
See detailed info → StandardATP2B1 · rs11105352
See detailed info → StandardHOXC4 · rs4759320
See detailed info → StandardSOX6 · rs12799126
See detailed info → StandardLSP1 · rs612652
See detailed info → StandardCLCN6 · rs6669371
See detailed info → StandardLOC100506393 · rs12829468
See detailed info → StandardLOC100506393 · rs4306343
See detailed info → StandardCLCN6 · rs149764880
See detailed info → StandardMECOM · rs988398
See detailed info → StandardRPP25 · rs12050759
See detailed info → StandardPLOD1 · rs72641011
See detailed info → StandardMOV10 · rs2999159
See detailed info → StandardKCNK3 · rs1275985
See detailed info →Showing 20 of 9061 · page 10 of 454
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.