8,408 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.
SAMHD1 · rs11696169
See detailed info → Standard on its ownMROH8 · rs73094911
See detailed info → Standard on its ownnear SRC · rs11697428
See detailed info → Standard on its ownLPL · rs7016529
See detailed info → Standard on its ownPRDM7 · rs117417690
See detailed info → Standard on its ownZNF341 · rs78382342
See detailed info → Standard on its ownMMP24 · rs2425025
See detailed info → Standard on its ownUQCC1 · rs62210588
See detailed info → Standard on its ownMTCL2 · rs73109224
See detailed info → Standard on its ownnear CBFA2T2 · rs17401449
See detailed info → Standard on its ownnear PHF20 · rs112043138
See detailed info → Standard on its ownnear KIF3B · rs77476644
See detailed info → Standard on its ownTM9SF4 · rs17093831
See detailed info → Standard on its ownC20orf203 · rs17123518
See detailed info → Standard on its ownSLA2 · rs55804368
See detailed info → Standard on its ownBPIFA2 · rs117186940
See detailed info → Standard on its ownSLC25A38P1 · rs12657787
See detailed info → Standard on its ownTEX41 · rs1830321
See detailed info → Standard on its ownCNDP2 · rs8084058
See detailed info → Standard on its ownPTPRR · rs10879211
See detailed info →Showing 20 of 8408 · page 26 of 421
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.