12,444 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.
CCDC88B · rs645078
See detailed info → SensitiveFADS2 · rs968567
See detailed info → SensitiveCD5/CD6 · rs79538630
See detailed info → SensitiveABCB5 · rs17143056
See detailed info → SensitiveSTAT4 · rs7582694
See detailed info → SensitiveAFF3 · rs12712067
See detailed info → SensitiveTATDN3 · rs11120029
See detailed info → SensitiveRGS1 · rs2816313
See detailed info → SensitiveFASLG · rs78037977
See detailed info → SensitiveBTN3A1 · rs4320356
See detailed info → SensitiveSTK39 · rs60587303
See detailed info → SensitiveIGF2AS · rs1004446
See detailed info → SensitivePRKD2 · rs402072
See detailed info → SensitiveTYK2 · rs34536443
See detailed info → SensitiveCD226 · rs1615504
See detailed info → SensitiveBCAR1 · rs8056814
See detailed info → SensitiveIL2RA · rs41295121
See detailed info → SensitiveIL2RA · rs10795791
See detailed info → SensitiveIKZF1 · rs62447205
See detailed info → SensitiveBACH2 · rs72928038
See detailed info →Showing 20 of 12444 · page 594 of 623
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.