7,184 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.
STXBP5 · rs9399599
See detailed info → Standard on its ownPDILT · rs12446492
See detailed info → Standard on its ownMAN2B1 · rs10411619
See detailed info → SensitiveCDYL2 · rs13329835
See detailed info → SensitiveCOX11 · rs6504950
See detailed info → SensitiveESR1 · rs3757318
See detailed info → Sensitivenear MRPS30 · rs10941679
See detailed info → SensitiveSSBP4 · rs4808801
See detailed info → SensitiveCCDC88C · rs941764
See detailed info → SensitiveDKFZp761E198 · rs3903072
See detailed info → SensitiveNTN4 · rs17356907
See detailed info → Sensitivenear ATF7IP · rs12422552
See detailed info → SensitivePRKCH · rs3783782
See detailed info → SensitivePADI4 · rs2301888
See detailed info → SensitiveAHNAK2 · rs2582532
See detailed info → SensitivePTPN2 · rs8083786
See detailed info → SensitiveRASGRP1 · rs8032939
See detailed info → SensitiveREL · rs34695944
See detailed info → SensitiveMTF1 · rs28411352
See detailed info → SensitiveLOC145837 · rs8026898
See detailed info →Showing 20 of 7184 · page 264 of 360
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.