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.
NEDD4 · rs1509406
See detailed info → StandardSMG6 · rs3760232
See detailed info → Sensitive on its ownTNIP1 · rs6579837
See detailed info → Standard on its ownFUT6 · rs12019136
See detailed info → StandardSPTB · rs75944157
See detailed info → Standard on its ownNDUFA11 · rs12974991
See detailed info → Standard on its ownCOL24A1 · rs11161721
See detailed info → Standard on its ownIGH · rs58087925
See detailed info → StandardPDE3A · rs112767900
See detailed info → Standard on its ownAZI1 · rs2659009
See detailed info → StandardADH1B · rs2066702
See detailed info → Standard on its ownNDUFA11 · rs12974440
See detailed info → Standard on its ownNDUFA11 · rs12980262
See detailed info → Standard on its ownNEO1 · rs1812835
See detailed info → Standard on its ownRGS6 · rs4899412
See detailed info → Standard on its ownRGS6 · rs2529471
See detailed info → Standard on its ownSOX9 · rs2193054
See detailed info → StandardATAD5 · rs79461387
See detailed info → StandardKANK2 · rs12974711
See detailed info → StandardEPS15L1 · rs875622
See detailed info →Showing 20 of 7431 · page 40 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.