10,866 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.
POLD3 · rs57796856
See detailed info → Sensitivenear SLC25A28 · rs2193352
See detailed info → SensitiveBMP5 · rs62404966
See detailed info → Sensitivenear SRSF3 · rs1321310
See detailed info → SensitiveFKBP5 · rs16878812
See detailed info → Sensitivenear DUSP10 · rs6658977
See detailed info → Sensitivenear WNT4 · rs72647484
See detailed info → Sensitivenear PTPN1 · rs1810502
See detailed info → SensitiveACTR1B · rs11692435
See detailed info → SensitiveNXN · rs73975588
See detailed info → Sensitivenear TET2 · rs17035289
See detailed info → SensitiveSMAD6 · rs4776316
See detailed info → SensitiveCOL4A2 · rs7993934
See detailed info → Sensitivenear BOC · rs12635946
See detailed info → Sensitivenear SATB2 · rs7593422
See detailed info → SensitiveMAMSTR · rs12979278
See detailed info → Sensitivenear PLCL1 · rs11893063
See detailed info → SensitiveFHL3 · rs61776719
See detailed info → Sensitivenear BMP2 · rs6085661
See detailed info → SensitiveRTEL1-TNFRSF6B · rs3787089
See detailed info →Showing 20 of 10866 · page 485 of 544
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.