7,519 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.
PITX2 · rs17570669
See detailed info → StandardCAV2 · rs17516287
See detailed info → StandardARHGAP26 · rs174048
See detailed info → StandardSLC35F1 · rs17079881
See detailed info → StandardMIR297 · rs149829837
See detailed info → StandardUSP3 · rs146311723
See detailed info → StandardKCND3 · rs1443926
See detailed info → StandardPITX2 · rs143269342
See detailed info → StandardGJA1 · rs13191450
See detailed info → StandardPITX2 · rs13105878
See detailed info → StandardFTO · rs9941349
See detailed info → StandardDNAH10 · rs12298484
See detailed info → StandardLINC00326 · rs12208899
See detailed info → StandardPRRX1 · rs12142379
See detailed info → StandardIL6R · rs12129500
See detailed info → StandardMETTL11B · rs12122060
See detailed info → StandardKCND3 · rs12044963
See detailed info → StandardCDK6 · rs11773884
See detailed info → StandardSUN1 · rs11768850
See detailed info → StandardPITX2 · rs112599895
See detailed info →Showing 20 of 7519 · page 364 of 376
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.