12,425 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.
SMAD3 · rs868036
See detailed info → SensitiveDACH1 · rs340561
See detailed info → SensitivePTPRD · rs62535767
See detailed info → SensitiveBTBD9 · rs61192259
See detailed info → SensitiveRNF8 · rs17636328
See detailed info → SensitiveATP2C1 · rs35987657
See detailed info → SensitiveDCDC2C · rs10208712
See detailed info → SensitivePTPRD · rs1975197
See detailed info → SensitivePTPRD · rs4626664
See detailed info → SensitiveBTBD9 · rs9296249
See detailed info → SensitiveBTBD9 · rs3923809
See detailed info → StandardGJA5 · rs79187193
See detailed info → StandardKCND3 · rs1545300
See detailed info → StandardMIR6500 · rs146518726
See detailed info → StandardAGBL4 · rs11590635
See detailed info → StandardHSPG2 · rs7529220
See detailed info → StandardXPO7 · rs7834729
See detailed info → StandardKCNH2 · rs7789146
See detailed info → StandardCDK6 · rs56201652
See detailed info → StandardKDM1B · rs34969716
See detailed info →Showing 20 of 12425 · page 614 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.