102,686 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.
TPCN1 · rs6489896
See detailed info → SensitiveSYNPR · rs116668122
See detailed info → SensitiveOARD1 · rs10947943
See detailed info → Sensitivenear KIAA2013 · rs6682554
See detailed info → SensitiveBIN1 · rs35114168
See detailed info → SensitivePRICKLE1 · rs896559
See detailed info → SensitiveDIO2-AS1 · rs7155666
See detailed info → SensitiveZFYVE1 · rs182804071
See detailed info → Sensitivenear BIN1 · rs6431220
See detailed info → SensitiveAPOE · rs72654463
See detailed info → SensitiveAPOE · rs72654461
See detailed info → SensitiveFERMT2 · rs74825460
See detailed info → SensitiveLEF1-AS1 · rs34710518
See detailed info → SensitiveSNX1 · rs3848143
See detailed info → SensitiveTOMM40 · rs115908094
See detailed info → StandardMARK4 · rs28607628
See detailed info → Standard on its ownnear GMNC · rs4686570
See detailed info → SensitiveOSBP2 · rs3804082
See detailed info → StandardAPOC1 · rs66807996
See detailed info → StandardCEACAM16-AS1 · rs138615096
See detailed info →Showing 20 of 79 · page 1 of 4
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.