8,408 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.
PTPN2 · rs2847297
See detailed info → StandardQSOX2 · rs7849585
See detailed info → StandardATP1B1 · rs1320976
See detailed info → Standard on its ownKCNJ2 · rs7219669
See detailed info → SensitiveB3GNT2 · rs11900673
See detailed info → SensitiveCSF2 · rs657075
See detailed info → StandardLEPR · rs1805096
See detailed info → SensitiveCSK · rs2289583
See detailed info → SensitiveTCF7 · rs4388254
See detailed info → SensitiveFCGR2A · rs6671847
See detailed info → SensitiveTYK2 · rs11085727
See detailed info → SensitiveUBE2L3 · rs3747093
See detailed info → SensitiveIRF7 · rs58688157
See detailed info → SensitivePRDM1 · rs6568431
See detailed info → SensitiveSTAT4 · rs6736175
See detailed info → SensitiveIRF8 · rs13332649
See detailed info → SensitiveTNIP1 · rs6889239
See detailed info → SensitiveIRF5 · rs3757387
See detailed info → SensitiveSMG7 · rs17849501
See detailed info → StandardTOMM40 · rs1160985
See detailed info →Showing 20 of 8408 · page 344 of 421
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.