12,469 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.
GSDMA · rs3894194
See detailed info → StandardFN3K · rs1046896
See detailed info → StandardGCK · rs1799884
See detailed info → StandardHLA-B · rs2395029
See detailed info → StandardTCF4 · rs1452787
See detailed info → StandardSLC12A9 · rs7801190
See detailed info → StandardIL33 · rs1342326
See detailed info → Sensitivenear EMSY · rs2155219
See detailed info → SensitiveCDC123 · rs10906115
See detailed info → Sensitivenear KLF5 · rs9600079
See detailed info → SensitiveGPRC6A · rs339331
See detailed info → SensitiveSNCA · rs356219
See detailed info → SensitiveMCCC1 · rs11711441
See detailed info → StandardGPRC6A · rs6901250
See detailed info → SensitiveVDR · rs11168249
See detailed info → SensitiveCXCR5 · rs630923
See detailed info → Sensitivenear TMEM135 · rs6592362
See detailed info → SensitiveRELA · rs2231884
See detailed info → StandardZNF648 · rs1689800
See detailed info → SensitiveDUXA · rs11672517
See detailed info →Showing 20 of 12469 · page 582 of 624
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.