8,005 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.
BATF3 · rs906364
See detailed info → StandardLINC00299 · rs10178845
See detailed info → StandardNRROS · rs7636495
See detailed info → SensitiveSAMD13 · rs2143757
See detailed info → StandardRPTN · rs12123821
See detailed info → StandardCASC15 · rs952579
See detailed info → StandardSESN1 · rs11759732
See detailed info → StandardAHI1 · rs4526212
See detailed info → StandardGSAP · rs2190097
See detailed info → SensitiveEMX1 · rs999494
See detailed info → SensitiveVRK2 · rs7596038
See detailed info → SensitiveRBKS · rs12623170
See detailed info → SensitiveFAM5B · rs6670165
See detailed info → SensitiveEGR1 · rs13164092
See detailed info → SensitiveCA8 · rs867743
See detailed info → SensitiveHYAL3 · rs2073499
See detailed info → SensitiveBTNL2 · rs116047537
See detailed info → StandardLINC00709 · rs72782676
See detailed info → SensitiveAMBRA1 · rs61882743
See detailed info → SensitiveLETM2 · rs112537273
See detailed info →Showing 20 of 8005 · page 254 of 401
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.