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.
PRDM16 · rs56304645
See detailed info → Standard on its ownnear PLEKHA1 · rs78438709
See detailed info → Standard on its ownASTN2 · rs17220352
See detailed info → SensitiveSEMA3 · rs117617821
See detailed info → SensitiveSEMA3 · rs62472985
See detailed info → Standard on its ownMARCHF1 · rs723730
See detailed info → Standard on its ownKANSL1 · rs80103986
See detailed info → StandardPRDM16 · rs2493292
See detailed info → Standard on its ownSLC8A1 · rs2110927
See detailed info → Standard on its ownGLIS1 · rs4926611
See detailed info → Standard on its ownERP27 · rs11614333
See detailed info → StandardTNRC6A · rs11639856
See detailed info → Standard on its ownMARCHF1 · rs6822628
See detailed info → SensitiveRET · rs17653445
See detailed info → Standard on its ownMARCHF1 · rs17044565
See detailed info → Sensitive on its ownZKSCAN3 · rs13213152
See detailed info → Sensitive on its ownOR2B3P · rs3129788
See detailed info → Sensitive on its ownMAS1L · rs1233491
See detailed info → Sensitive on its ownZNRD1 · rs8321
See detailed info → Sensitive on its ownSTK19 · rs389884
See detailed info →Showing 20 of 7670 · page 37 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.