8,529 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.
LPXN · rs12289961
See detailed info → Standard on its ownLAMB1 · rs2072209
See detailed info → StandardGNPDA2 · rs348495
See detailed info → StandardACTN1 · rs434943
See detailed info → Standard on its ownSMARCB1 · rs2186369
See detailed info → Standard on its ownSASH1 · rs9497965
See detailed info → StandardITPK1 · rs8006385
See detailed info → StandardZNF365 · rs10995251
See detailed info → StandardC14orf70 · rs7149242
See detailed info → StandardRPH3A · rs17824620
See detailed info → StandardRAD51L1 · rs8022206
See detailed info → StandardSNORD7 · rs10512472
See detailed info → StandardITIH4 · rs2535633
See detailed info → StandardTAOK1 · rs559972
See detailed info → StandardAKAP10 · rs397969
See detailed info → StandardC14orf73 · rs2297067
See detailed info → StandardPRKAG2 · rs10480300
See detailed info → StandardHK1 · rs10159477
See detailed info → StandardACOXL · rs10207392
See detailed info → StandardHBS1L · rs9389269
See detailed info →Showing 20 of 8529 · page 341 of 427
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.