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.
APOC1 · rs66807996
See detailed info → StandardCEACAM16-AS1 · rs138615096
See detailed info → SensitiveTREML2 · rs9394766
See detailed info → Sensitivenear RNU6-560P · rs1898895
See detailed info → SensitiveLNCOB1 · rs166907
See detailed info → StandardAPOE · rs769451
See detailed info → Standardnear ZNF285 · rs2722753
See detailed info → SensitiveSORL1 · rs117807585
See detailed info → StandardLNCOB1 · rs116967764
See detailed info → SensitiveAPOE · rs435380
See detailed info → SensitiveAPOE · rs446037
See detailed info → StandardAPOC1P1 · rs11878790
See detailed info → StandardIGSF23 · rs11668972
See detailed info → StandardCEACAM16-AS1 · rs2965163
See detailed info → Standardnear CBLC · rs187010311
See detailed info → StandardTOMM40 · rs552796536
See detailed info → StandardRELB · rs562844449
See detailed info → StandardNECTIN2 · rs527428691
See detailed info → Sensitivenear TREML2 · rs60755019
See detailed info → SensitiveLINC01234 · rs111486601
See detailed info →Showing 20 of 81 · page 2 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.