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.
PRPH2 · rs649472
See detailed info → SensitiveSLC35D4 · rs10502437
See detailed info → SensitiveLTBP1 · rs2061027
See detailed info → SensitiveTGFB1 · rs75621460
See detailed info → SensitiveNF1 · rs2953013
See detailed info → SensitiveFGF10 · rs2121875
See detailed info → SensitiveGLIS3 · rs10974438
See detailed info → Sensitivenear COL27A1 · rs919642
See detailed info → Sensitivenear CDC5L · rs12154055
See detailed info → SensitiveHLA-DPB1 · rs2856821
See detailed info → SensitiveH2BC4 · rs115740542
See detailed info → SensitiveSCUBE1 · rs528981060
See detailed info → SensitiveUQCC1 · rs2248393
See detailed info → Sensitivenear ZC3H11B · rs2785988
See detailed info → Sensitivenear CSK · rs35206230
See detailed info → StandardSLC47A1 · rs2453580
See detailed info → StandardUMOD · rs13329952
See detailed info → StandardINO80 · rs476633
See detailed info → StandardWDR37 · rs1044261
See detailed info → StandardSTC1 · rs3758086
See detailed info →Showing 20 of 7670 · page 227 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.