12,505 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.
SERPINF2 · rs11078597
See detailed info → StandardPDIA4 · rs822552
See detailed info → StandardSEPT2 · rs12694997
See detailed info → StandardCCDC53/GNPTAB · rs7971536
See detailed info → SensitiveGLIS3 · rs10814916
See detailed info → SensitiveFAM58A · rs12010175
See detailed info → SensitiveHEATR3 · rs4785204
See detailed info → SensitiveGRK5 · rs10886471
See detailed info → StandardC9orf64 · rs7853377
See detailed info → StandardSLC38A9 · rs11958779
See detailed info → StandardEIF2AK3 · rs11684404
See detailed info → StandardNCKAP5 · rs7567288
See detailed info → StandardPRKG2/BMP3 · rs788867
See detailed info → StandardFHL5 · rs11759769
See detailed info → SensitiveC1orf106 · rs7522462
See detailed info → SensitiveBACH2 · rs12212193
See detailed info → SensitiveAHI1 · rs11154801
See detailed info → SensitiveAFF3 · rs7583877
See detailed info → SensitiveMCTP2 · rs12437854
See detailed info → StandardITGA4 · rs2124440
See detailed info →Showing 20 of 12505 · page 552 of 626
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.