8,838 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.
AHRR · rs62330027
See detailed info → Standard on its ownAKAP13 · rs62024517
See detailed info → Standard on its ownDNM1P35 · rs17424999
See detailed info → Standard on its ownMIR5011 · rs181331502
See detailed info → Standard on its ownGPR158 · rs10508700
See detailed info → Standard on its ownNEURL1 · rs72848971
See detailed info → Standard on its ownWBP4 · rs78169557
See detailed info → Standard on its ownNEDD4 · rs1912403
See detailed info → Standard on its ownUBE2L3 · rs5754102
See detailed info → SensitiveTAMM41 · rs142823282
See detailed info → Standard on its ownKALRN · rs6776396
See detailed info → SensitiveDDR1 · rs118124843
See detailed info → Standard on its ownLUM · rs57812022
See detailed info → Standard on its ownMECOM · rs34781085
See detailed info → Standard on its ownISOC1 · rs11952939
See detailed info → SensitiveSNCAIP · rs149641852
See detailed info → Standard on its ownSPRED2 · rs12713563
See detailed info → Standard on its ownDNALI1 · rs4653301
See detailed info → Standard on its ownSPTBN1 · rs76070960
See detailed info → Standard on its ownKALRN · rs986912
See detailed info →Showing 20 of 8838 · page 15 of 442
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.