12,427 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.
DERA · rs151326733
See detailed info → StandardTXNRD2 · rs73148965
See detailed info → StandardPDE7B · rs9494457
See detailed info → StandardLOC107986141 · rs11710139
See detailed info → StandardMECOM · rs73174345
See detailed info → StandardMYOF · rs61861119
See detailed info → StandardANGPT1 · rs10505100
See detailed info → StandardTHSD7A · rs12699251
See detailed info → StandardARHGEF12 · rs58073046
See detailed info → StandardLOC100147773 · rs7518099
See detailed info → StandardANGPT1 · rs2022945
See detailed info → StandardMIR4776-1 · rs62188040
See detailed info → StandardGAS7 · rs9913911
See detailed info → StandardCADM2 · rs66500121
See detailed info → StandardELP4 · rs555091
See detailed info → StandardCDKN2BAS · rs523096
See detailed info → StandardETFDH · rs8396
See detailed info → StandardIL29 · rs8099917
See detailed info → Standard on its ownICAM1 · rs1799969
See detailed info → SensitiveKITLG · rs995030
See detailed info →Showing 20 of 12427 · page 605 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.