7,604 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.
MBNL1 · rs182314334
See detailed info → StandardKBTBD2 · rs3750082
See detailed info → StandardTSPAN9 · rs10491967
See detailed info → StandardSIPA1L3 · rs11666497
See detailed info → StandardACAN · rs28584580
See detailed info → Standard on its ownLOC100129340 · rs7031417
See detailed info → StandardACCN2 · rs11614785
See detailed info → StandardADAMTS17 · rs4988781
See detailed info → StandardACAN · rs3817428
See detailed info → StandardACAN · rs11856122
See detailed info → SensitiveZSCAN31 · rs13217619
See detailed info → Sensitivenear SPATS2L · rs1367858
See detailed info → SensitivePOM121L2 · rs13217239
See detailed info → SensitiveGRIA1 · rs13170232
See detailed info → SensitiveFXR1 · rs13096210
See detailed info → Sensitivenear NMB · rs12908161
See detailed info → SensitiveCACNA1C · rs12823424
See detailed info → Sensitivenear GRIA1 · rs12522290
See detailed info → Sensitivenear LUZP2 · rs12360997
See detailed info → Sensitivenear RPP21 · rs114200269
See detailed info →Showing 20 of 7604 · page 225 of 381
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.