7,839 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.
near CST8 · rs113118940
See detailed info → SensitiveTMC5 · rs118099348
See detailed info → Sensitivenear CST1 · rs147525344
See detailed info → Sensitivenear ATP2B1 · rs117483990
See detailed info → Sensitivenear NRG3 · rs190780914
See detailed info → Sensitivenear SLC16A9 · rs61860854
See detailed info → Sensitivenear JCAD · rs146650065
See detailed info → SensitiveTMEM132C · rs144288546
See detailed info → Sensitivenear HSD17B12 · rs139675748
See detailed info → SensitiveNKAIN3 · rs4557697
See detailed info → SensitivePHF14 · rs183600932
See detailed info → SensitiveKDM1B · rs188911996
See detailed info → StandardSLC22A4 · rs12777
See detailed info → StandardFGG · rs76289367
See detailed info → StandardC5orf56 · rs2057655
See detailed info → StandardZFP36L1 · rs367677
See detailed info → StandardFGG · rs148685782
See detailed info → StandardFGB · rs6054
See detailed info → StandardFGB · rs150768229
See detailed info → StandardTTC17 · rs7934094
See detailed info →Showing 20 of 7839 · page 230 of 392
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.