9,570 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.
CCDC92 · rs3789967
See detailed info → StandardBEST3 · rs35349325
See detailed info → StandardMTSS1 · rs35006907
See detailed info → StandardKCNN3 · rs34292822
See detailed info → StandardSPATS2L · rs295114
See detailed info → StandardNAV2 · rs2625322
See detailed info → StandardPITX2 · rs2595104
See detailed info → StandardMAPT · rs242557
See detailed info → StandardLRIG1 · rs2306272
See detailed info → StandardAKAP6 · rs2145587
See detailed info → StandardUBE4B · rs187585530
See detailed info → StandardPITX2 · rs17570669
See detailed info → StandardCAV2 · rs17516287
See detailed info → StandardARHGAP26 · rs174048
See detailed info → StandardSLC35F1 · rs17079881
See detailed info → StandardMIR297 · rs149829837
See detailed info → StandardUSP3 · rs146311723
See detailed info → StandardKCND3 · rs1443926
See detailed info → StandardPITX2 · rs143269342
See detailed info → StandardGJA1 · rs13191450
See detailed info →Showing 20 of 9570 · page 466 of 479
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.