9,424 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.
METTL11B · rs12122060
See detailed info → StandardKCND3 · rs12044963
See detailed info → StandardCDK6 · rs11773884
See detailed info → StandardSUN1 · rs11768850
See detailed info → StandardPITX2 · rs112599895
See detailed info → StandardLINC00477 · rs10842383
See detailed info → StandardPSMB7 · rs10760361
See detailed info → StandardFAM13B · rs10479177
See detailed info → StandardC10orf76 · rs1044258
See detailed info → StandardSNRNP27 · rs10165883
See detailed info → StandardARHGAP10 · rs10027347
See detailed info → StandardMEX3C · rs9963878
See detailed info → StandardZFHX3 · rs876727
See detailed info → StandardRPL3L · rs77316573
See detailed info → StandardNACA · rs11614818
See detailed info → StandardLINC00477 · rs2291437
See detailed info → StandardNEURL1 · rs55693294
See detailed info → StandardHSF2 · rs9401451
See detailed info → StandardHAND2 · rs10520260
See detailed info → StandardPITX2 · rs138311480
See detailed info →Showing 20 of 9424 · page 460 of 472
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.