12,425 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.
JAZF1 · rs849135
See detailed info → StandardAFAP1 · rs4619890
See detailed info → StandardGMDS · rs11969985
See detailed info → StandardHLA-DPA3 · rs9366816
See detailed info → Standard on its ownASTN2 · rs562775223
See detailed info → Standard on its ownMIS18BP1 · rs555376144
See detailed info → Standard on its ownLSP1P3 · rs144414988
See detailed info → Standard on its ownACOT9 · rs761804508
See detailed info → Standard on its ownFRMPD4 · rs144371252
See detailed info → StandardNFE2L3 · rs10261878
See detailed info → Standard on its ownZNF804A · rs775583810
See detailed info → Standard on its ownC5orf63 · rs145648292
See detailed info → SensitiveDAZL · rs10510452
See detailed info → SensitiveCENPE · rs2720460
See detailed info → StandardSHROOM3 · rs4859682
See detailed info → StandardSUV420H1 · rs4930561
See detailed info → StandardMICA · rs6932730
See detailed info → StandardMIR548AR · rs183131780
See detailed info → StandardLOC730100 · rs6750228
See detailed info → StandardNR5A2 · rs12727980
See detailed info →Showing 20 of 12425 · page 516 of 622
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.