8,107 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.
CACNA1I · rs5750854
See detailed info → Standard on its ownPREX1 · rs6095298
See detailed info → Standard on its ownENSG00000212569 · rs10854884
See detailed info → Standard on its ownARFGEF2 · rs6095360
See detailed info → Standard on its ownARFGEF2 · rs13044144
See detailed info → Standard on its ownARFGEF2 · rs3092566
See detailed info → Standard on its ownZNF335 · rs3092073
See detailed info → Standard on its ownSTAU1 · rs2426132
See detailed info → Standard on its ownSHANK3 · rs5770820
See detailed info → Standard on its ownLARGE · rs11703032
See detailed info → Standard on its ownRASD2 · rs13053308
See detailed info → Standard on its ownENSG00000267780 · rs11664298
See detailed info → Standard on its ownDCC · rs7506451
See detailed info → Standard on its ownDDX27 · rs6125597
See detailed info → Standard on its ownMAST1 · rs56160517
See detailed info → Standard on its ownENSG00000226956 · rs1389993
See detailed info → Standard on its ownCACNA1I · rs132570
See detailed info → Standard on its ownPHACTR3 · rs6027005
See detailed info → Standard on its ownDCC · rs12960505
See detailed info → Standard on its ownNFIX · rs11555274
See detailed info →Showing 20 of 8107 · page 29 of 406
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.