7,670 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.
LYPLAL1 · rs2605100
See detailed info → StandardMSRA · rs7826222
See detailed info → StandardTFAP2B · rs987237
See detailed info → StandardKCNMA1 · rs2116830
See detailed info → StandardSLC35F1 · rs281868
See detailed info → StandardPKD2L2 · rs6864727
See detailed info → StandardCEP68 · rs2723064
See detailed info → StandardMETTL11B · rs10800507
See detailed info → StandardDMRTA2 · rs56202902
See detailed info → StandardGIPR · rs10423928
See detailed info → StandardZHFX3 · rs4404097
See detailed info → StandardPITX2 · rs77831929
See detailed info → StandardTTN · rs12614435
See detailed info → StandardPPFIA4 · rs3737883
See detailed info → StandardABCA1 · rs1883025
See detailed info → SensitiveCD69 · rs4763879
See detailed info → Standard on its ownSLC16A9 · rs12356193
See detailed info → Standard on its ownDCDC5 · rs3925584
See detailed info → SensitiveELF1 · rs7329174
See detailed info → Standard on its ownATOH7 · rs3858145
See detailed info →Showing 20 of 7670 · page 378 of 384
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.