7,519 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.
ASAP3 · rs1077514
See detailed info → SensitiveSUMO1P1 · rs6022786
See detailed info → SensitiveHMGA2 · rs2272046
See detailed info → SensitiveYAP1 · rs1894116
See detailed info → SensitiveC9orf3 · rs3802457
See detailed info → SensitiveHHAT · rs7527939
See detailed info → SensitiveSP4 · rs2285947
See detailed info → Sensitivenear POU5F1B · rs10505483
See detailed info → Sensitivenear POU5F1B · rs6983561
See detailed info → Standard on its ownMLXIPL · rs7800944
See detailed info → Standard on its ownEFCAB5 · rs9902453
See detailed info → Standard on its ownDUSP1 · rs17658229
See detailed info → SensitiveSLC24A4 · rs10498633
See detailed info → Standard on its ownITGA1 · rs4074793
See detailed info → Standard on its ownLYRM9 · rs3751972
See detailed info → StandardSTXBP5 · rs9399599
See detailed info → Standard on its ownPDILT · rs12446492
See detailed info → Standard on its ownMAN2B1 · rs10411619
See detailed info → SensitiveCDYL2 · rs13329835
See detailed info → SensitiveCOX11 · rs6504950
See detailed info →Showing 20 of 7519 · page 280 of 376
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.