12,426 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.
LBH · rs17321999
See detailed info → SensitiveTNPO3 · rs12539741
See detailed info → SensitiveTNIP1 · rs7708392
See detailed info → SensitiveITGAM · rs1143679
See detailed info → SensitiveUBE2L3 · rs7444
See detailed info → SensitiveTYK2 · rs2304256
See detailed info → SensitivePLD2 · rs2286672
See detailed info → SensitiveITGAM · rs34572943
See detailed info → SensitiveDHCR7 · rs3794060
See detailed info → SensitiveIRF7 · rs12802200
See detailed info → SensitiveTNFAIP3 · rs6932056
See detailed info → SensitiveUHRF1BP1 · rs9462027
See detailed info → SensitiveIRF8 · rs11644034
See detailed info → SensitiveMIR146A · rs2431697
See detailed info → SensitiveTCF7 · rs7726414
See detailed info → SensitiveBANK1 · rs10028805
See detailed info → SensitiveIL12A · rs564799
See detailed info → SensitiveABHD6 · rs9311676
See detailed info → SensitiveTNFSF4 · rs704840
See detailed info → SensitiveAFF1 · rs340630
See detailed info →Showing 20 of 12426 · page 498 of 622
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.