9,493 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.
ARB2A · rs72786644
See detailed info → StandardMEF2C · rs34316
See detailed info → Standardnear NR2F1 · rs114468556
See detailed info → Standardnear MAN2A1 · rs2416214
See detailed info → StandardMCC · rs4705763
See detailed info → Standardnear IRX1 · rs16871807
See detailed info → Standardnear IRX2 · rs10475186
See detailed info → StandardCTNND2 · rs31940
See detailed info → Standardnear GALNTL6 · rs13117856
See detailed info → Standardnear MFAP3L · rs1904823
See detailed info → StandardASB5 · rs2624881
See detailed info → StandardTMEM267 · rs4242099
See detailed info → StandardGATB · rs6823423
See detailed info → StandardPDGFC · rs983473
See detailed info → StandardMAML3 · rs35612722
See detailed info → Standardnear RAPGEF2 · rs11100237
See detailed info → Standardnear FST · rs62370510
See detailed info → Standardnear NOCT · rs11726181
See detailed info → StandardTMEM192 · rs34316562
See detailed info → Standardnear ARL15 · rs702606
See detailed info →Showing 20 of 9493 · page 6 of 475
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.