8,288 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.
FOXP1 · rs2116709
See detailed info → SensitiveRGS22 · rs141115006
See detailed info → Standard on its ownSELP · rs6703865
See detailed info → StandardZNF652 · rs12940887
See detailed info → Standard on its ownPOC1B · rs11105298
See detailed info → Standard on its ownMTHFR · rs3753584
See detailed info → Standard on its ownNPPB · rs198379
See detailed info → StandardBAT2 · rs2187668
See detailed info → StandardPLEKHG1 · 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 →Showing 20 of 8288 · page 247 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.