102,854 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.
APOE · rs115299243
See detailed info → StandardAPOE/C1/C2/C4 · rs141622900
See detailed info → StandardAPOE · rs10414043
See detailed info → StandardAPOC1 · rs12721046
See detailed info → StandardAPOE · rs438811
See detailed info → StandardTOMM40 · rs71352238
See detailed info → StandardAPOE · rs483082
See detailed info → StandardPVRL2 · rs12972970
See detailed info → StandardTOMM40 · rs34095326
See detailed info → StandardTOMM40 · rs184017
See detailed info → StandardTOMM40 · rs10119
See detailed info → StandardTOMM40 · rs157582
See detailed info → StandardPVRL2 · rs283815
See detailed info → Sensitivenear USP6NL · rs11257238
See detailed info → StandardAPOE · rs769449
See detailed info → StandardAPOE · rs7412
See detailed info → StandardAPOE · rs12721051
See detailed info → SensitiveAPOE · rs429358
See detailed info → StandardAPOE · rs4420638
See detailed info → SensitiveAPOE · rs2075650
See detailed info →Showing 20 of 81 · page 4 of 5
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.