12,524 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.
PAPPA2 · rs1325598
See detailed info → StandardPIP4K2B · rs1043515
See detailed info → StandardPDS5B/BRCA2 · rs7332115
See detailed info → StandardTEAD1 · rs7926971
See detailed info → StandardRHOD · rs7112925
See detailed info → StandardNME2 · rs4605213
See detailed info → StandardTREH · rs494459
See detailed info → SensitiveIL22RA2 · rs17066096
See detailed info → SensitiveMMEL1 · rs4648356
See detailed info → SensitiveMYC · rs11780156
See detailed info → SensitiveARHGEF5 · rs720475
See detailed info → SensitiveCD86 · rs9282641
See detailed info → SensitiveRANBP9 · rs204247
See detailed info → StandardNELL-1 · rs12279250
See detailed info → SensitiveGPR65 · rs2119704
See detailed info → StandardZNF676 · rs412658
See detailed info → SensitiveCHEK2 · rs4822983
See detailed info → StandardCTC1 · rs3027234
See detailed info → SensitiveCLECL1 · rs10466829
See detailed info → Sensitivenear FGFR2 · rs11199914
See detailed info →Showing 20 of 12524 · page 548 of 627
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.