7,592 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.
THADA · rs7578597
See detailed info → SensitiveLGR5 · rs7961581
See detailed info → SensitiveJAZF1 · rs864745
See detailed info → SensitiveCHRNA5 · rs8034191
See detailed info → StandardMATP · rs35391
See detailed info → StandardNOS1AP · rs12029454
See detailed info → SensitiveCXCL12 · rs1746048
See detailed info → StandardCITED2 · rs628751
See detailed info → SensitivePHACTR1 · rs12526453
See detailed info → SensitiveSLC4A7 · rs4973768
See detailed info → Standard on its ownG6PC2 · rs560887
See detailed info → SensitiveBMP4 · rs4444235
See detailed info → SensitiveKCNQ1 · rs2237897
See detailed info → Standard on its ownCAV1 · rs3807989
See detailed info → SensitiveKIAA0350 · rs12708716
See detailed info → StandardTRIB1 · rs2954029
See detailed info → StandardLPL · rs12678919
See detailed info → SensitiveMAP2K5 · rs12593813
See detailed info → StandardGALNT2 · rs4846914
See detailed info → SensitiveEHBP1 · rs721048
See detailed info →Showing 20 of 7592 · page 376 of 380
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.