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.
PLTP · 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 → StandardCITED2 · rs628751
See detailed info → SensitivePHACTR1 · rs12526453
See detailed info → SensitiveSLC4A7 · rs4973768
See detailed info → Standard on its ownG6PC2 · rs560887
See detailed info → SensitiveBMP4 · rs4444235
See detailed info → SensitiveKCNQ1 · rs2237897
See detailed info →Showing 20 of 7519 · page 372 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.