8,698 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.
DCHS2 · rs2045323
See detailed info → SensitiveSTK39 · rs1474055
See detailed info → SensitiveSIPA1L2 · rs10797576
See detailed info → Standard on its ownESR1 · rs3020331
See detailed info → StandardDLG4 · rs314253
See detailed info → Standard on its ownCCDC27 · rs1175550
See detailed info → Standard on its ownPSMB4 · rs2769264
See detailed info → StandardFTO · rs62033400
See detailed info → SensitiveBRIP1 · rs34289250
See detailed info → StandardMPP3 · rs8077889
See detailed info → StandardHBS1L · rs9376090
See detailed info → StandardCDCA7 · rs10930597
See detailed info → StandardGPR146 · rs1997243
See detailed info → Standard on its ownCYP19A1 · rs2414095
See detailed info → StandardPLEKHG1 · rs17080102
See detailed info → StandardCBX7 · rs877529
See detailed info → SensitiveADAM15 · rs1218582
See detailed info → SensitiveTBX5 · rs1270884
See detailed info → SensitiveNGFR · rs11650494
See detailed info → SensitiveLACE1 · rs2273669
See detailed info →Showing 20 of 8698 · page 316 of 435
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.