12,423 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.
LILRA3 · rs103294
See detailed info → StandardPEPD · rs4805885
See detailed info → StandardRUNX1 · rs150498232
See detailed info → Standard on its ownMAG13 · rs1230666
See detailed info → StandardC20orf203 · rs6058796
See detailed info → StandardPRTN3 · rs56757486
See detailed info → SensitiveNDST3 · rs11098403
See detailed info → SensitiveSALM1 · rs34517613
See detailed info → StandardCA5A · rs8056952
See detailed info → StandardZFPM1 · rs12447180
See detailed info → StandardVMP1 · rs1292061
See detailed info → StandardFUT6 · rs778798
See detailed info → StandardANGPTL1 · rs4650994
See detailed info → SensitiveABHD6 · rs73081554
See detailed info → StandardADH5 · rs2602836
See detailed info → SensitiveCEP57 · rs4409785
See detailed info → SensitiveCOG6 · rs9603616
See detailed info → StandardABCF2 · rs1122979
See detailed info → StandardMTMR3 · rs5763662
See detailed info → StandardLRPAP1 · rs6831256
See detailed info →Showing 20 of 12423 · page 528 of 622
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.