10,875 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.
LOC389936 · rs12247397
See detailed info → SensitiveESR1 · rs2046210
See detailed info → Standard on its ownSCARB1 · rs11057830
See detailed info → SensitiveCANCNA1C · rs4765913
See detailed info → StandardSLC4A7 · rs13082711
See detailed info → SensitiveZFP36L2 · rs12478601
See detailed info → StandardMTCH2 · rs10838738
See detailed info → StandardAPOB · rs693
See detailed info → StandardABCA1 · rs3905000
See detailed info → Standard on its ownHLA-DQB1 · rs9357152
See detailed info → StandardARMC2 · rs2798641
See detailed info → StandardMMP15 · rs12447804
See detailed info → StandardZKSCAN3 · rs6903823
See detailed info → StandardGRIN2A · rs11866328
See detailed info → StandardABO · rs495828
See detailed info → SensitiveF11 · rs3756008
See detailed info → Standard on its ownPSMB9 · rs2187689
See detailed info → Standard on its ownPARK2 · rs926849
See detailed info → Standard on its ownGIPR · rs11671664
See detailed info → StandardTMEM38B · rs1516883
See detailed info →Showing 20 of 10875 · page 482 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.