8,005 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.
TYR · rs1393350
See detailed info → SensitiveUnknown · rs3764147
See detailed info → Standard on its ownTCHH · rs17646946
See detailed info → StandardTYR · rs1847134
See detailed info → SensitiveRYR3 · rs2229116
See detailed info → Standard on its ownACADM · rs211718
See detailed info → StandardPLTP · rs7679
See detailed info → StandardKCNJ2 · rs17779747
See detailed info → StandardKCNH2 · rs2968863
See detailed info → StandardATP1B1 · rs10919071
See detailed info → StandardTBL2 · rs17145738
See detailed info → SensitiveIL12A · rs17810546
See detailed info → SensitiveECHDC1 · rs2180341
See detailed info → SensitiveTHADA · rs7578597
See detailed info → SensitiveLGR5 · rs7961581
See detailed info → SensitiveJAZF1 · rs864745
See detailed info → SensitiveCHRNA5 · rs8034191
See detailed info → StandardMATP · rs35391
See detailed info → StandardNOS1AP · rs12029454
See detailed info → SensitiveCXCL12 · rs1746048
See detailed info →Showing 20 of 8005 · page 396 of 401
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.