12,444 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.
PTPRC · rs7555082
See detailed info → SensitiveSPMIP7 · rs12718244
See detailed info → SensitiveSLAIN2 · rs7438704
See detailed info → SensitiveGPR18 · rs3742130
See detailed info → SensitiveNDFIP1 · rs6863411
See detailed info → Sensitivenear TRIB1 · rs921720
See detailed info → SensitiveADAM30 · rs2641348
See detailed info → SensitiveAKAP11 · rs80244186
See detailed info → SensitiveZNF365 · rs224143
See detailed info → SensitiveHLA-DQB1 · rs140068907
See detailed info → SensitiveTNFSF15 · rs6478109
See detailed info → SensitiveHLA-B · rs114985235
See detailed info → SensitiveIL3 · rs3091338
See detailed info → SensitiveSLC43A3 · rs11229030
See detailed info → SensitiveC8orf84 · rs12677663
See detailed info → SensitiveUBD · rs9258260
See detailed info → SensitiveSLCO6A1 · rs7705924
See detailed info → SensitiveTMEM17 · rs6545946
See detailed info → SensitiveMAGI1 · rs11924265
See detailed info → Sensitivenear PPP5C · rs4802307
See detailed info →Showing 20 of 12444 · page 596 of 623
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.