7,670 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.
BHMT · rs617219
See detailed info → Sensitivenear HLA-DRA · rs187696124
See detailed info → Sensitivenear SMIM38 · rs10896449
See detailed info → StandardCCDC27 · rs1181870
See detailed info → StandardADCY8 · rs17311976
See detailed info → StandardFAT1 · rs148750727
See detailed info → StandardAPH1A · rs10157197
See detailed info → StandardAK5 · rs76681500
See detailed info → StandardLINC01128 · rs141175086
See detailed info → StandardFCGR2B · rs61804164
See detailed info → StandardDNM3 · rs554019
See detailed info → StandardGDF5 · rs6060373
See detailed info → SensitiveLTBP1 · rs4630744
See detailed info → SensitiveTGFA · rs3821262
See detailed info → SensitiveSLBP · rs11732213
See detailed info → SensitiveHLA-DPB1 · rs9277552
See detailed info → StandardPAPPA2 · rs61823001
See detailed info → StandardADAMTS7 · rs62011052
See detailed info → StandardGATA2 · rs62270945
See detailed info → Sensitivenear CAVIN2 · rs12470967
See detailed info →Showing 20 of 7670 · page 226 of 384
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.