10,913 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.
RHPN2 · rs10411210
See detailed info → SensitivePOU2AF3 · rs3802842
See detailed info → SensitiveTGFB1 · rs1800469
See detailed info → SensitiveAS1 · rs704017
See detailed info → SensitivePLCB1 · rs2423279
See detailed info → SensitiveNABP1 · rs11903757
See detailed info → StandardAKR1C4 · rs182498797
See detailed info → Standardnear CENPW · rs9401883
See detailed info → Standardnear LIN28B · rs2095812
See detailed info → StandardC11orf63 · rs144048300
See detailed info → StandardPTPRD · rs291269
See detailed info → StandardBRCA1 · rs1799949
See detailed info → StandardMSH5-SAPCD1 · rs707938
See detailed info → StandardSYCP2L · rs9393800
See detailed info → StandardOLFM2 · rs889122
See detailed info → StandardEVI5L · rs652260
See detailed info → StandardDLGAP1 · rs12607903
See detailed info → StandardKCTD13 · rs1129700
See detailed info → StandardDET1 · rs12915845
See detailed info → StandardRORA · rs3743266
See detailed info →Showing 20 of 10913 · page 490 of 546
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.