8,005 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 · rs11118316
See detailed info → Standard on its ownCHRNA5 · rs2036527
See detailed info → Standard on its ownTNFRSF13B · rs4792800
See detailed info → Standard on its ownESR1 · rs12173570
See detailed info → StandardENPEP · rs6825911
See detailed info → StandardSLC2A9 · rs11722228
See detailed info → StandardABCG2 · rs4148155
See detailed info → StandardSLC22A12 · rs506338
See detailed info → StandardCSF3 · rs4065321
See detailed info → SensitiveTERT · rs2242652
See detailed info → StandardCDK6 · rs445
See detailed info → SensitiveLRRK2 · rs34637584
See detailed info → Standard on its ownSCARB1 · rs10846744
See detailed info → StandardMIPEP · rs9318086
See detailed info → SensitiveCSNK1A1 · rs10058728
See detailed info → SensitiveHCP5 · rs9469003
See detailed info → SensitiveRIN3 · rs10498635
See detailed info → Standard on its ownSLC6A20 · rs17279437
See detailed info → SensitiveIGF2BP2 · rs1470579
See detailed info → SensitiveHNF1A · rs7957197
See detailed info →Showing 20 of 8005 · page 351 of 401
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.