8,300 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.
PLEKHG1 · rs17080093
See detailed info → StandardCHRNB4 · rs11072791
See detailed info → StandardAGT · rs2493134
See detailed info → StandardST7L · rs1620668
See detailed info → StandardMTHFR · rs17037390
See detailed info → StandardCRYAA · rs12627651
See detailed info → StandardELAVL3 · rs17638167
See detailed info → StandardINSR · rs4247374
See detailed info → StandardLRRC10B · rs751984
See detailed info → Standard on its ownRGS10 · rs10510057
See detailed info → StandardCHRNB4 · rs4886579
See detailed info → StandardCHRNB4 · rs922692
See detailed info → StandardIREB2 · rs1062980
See detailed info → Standardnear HHIP · rs6537293
See detailed info → StandardFIGN · rs1371182
See detailed info → StandardCHRNB4 · rs4887077
See detailed info → StandardCHRNB4 · rs2170311
See detailed info → Standardnear GYPA · rs6834183
See detailed info → StandardFAM13A · rs2045517
See detailed info → StandardDBH · rs1108581
See detailed info →Showing 20 of 8300 · page 248 of 415
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.