7,839 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.
LSP1P3 · rs144414988
See detailed info → Standard on its ownACOT9 · rs761804508
See detailed info → Standard on its ownFRMPD4 · rs144371252
See detailed info → Standard on its ownASTN2 · rs562775223
See detailed info → Standard on its ownZNF804A · rs775583810
See detailed info → Standard on its ownC5orf63 · rs145648292
See detailed info → StandardSHROOM3 · rs4859682
See detailed info → SensitiveDAZL · rs10510452
See detailed info → SensitiveCENPE · rs2720460
See detailed info → Standard on its ownSUV420H1 · rs4930561
See detailed info → StandardLOC730100 · rs6750228
See detailed info → Standard on its ownMICA · rs6932730
See detailed info → StandardMIR548AR · rs183131780
See detailed info → StandardNR5A2 · rs12727980
See detailed info → StandardPAM · rs526231
See detailed info → StandardETV6 · rs2856321
See detailed info → StandardPEX2 · rs6473015
See detailed info → StandardPCCB · rs9844666
See detailed info → StandardADAM28 · rs1013209
See detailed info → StandardLYPLAL1 · rs11118346
See detailed info →Showing 20 of 7839 · page 287 of 392
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.