9,061 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.
VKORC1 · rs9923231
See detailed info → SensitiveHFE · rs1800562
See detailed info → StandardAR · rs6152
See detailed info → StandardABO · rs8176719
See detailed info → StandardDARC / ACKR1 · rs2814778
See detailed info → StandardCCR5 · rs333
See detailed info → SensitiveSLCO1B1 · rs4149056
See detailed info → StandardFUT2 · rs601338
See detailed info → StandardTAS2R38 · rs713598
See detailed info → Standard on its ownACTN3 · rs1815739
See detailed info → StandardALDH2 · rs671
See detailed info → StandardABCC11 · rs17822931
See detailed info → StandardSLC45A2 · rs16891982
See detailed info → StandardHERC2 / OCA2 · rs12913832
See detailed info → StandardADH1B · rs1229984
See detailed info → StandardCYP1A2 · rs762551
See detailed info → StandardMCM6 / LCT · rs4988235
See detailed info → SensitiveF5 · rs6025
See detailed info → StandardMTHFR · rs1801133
See detailed info → StandardOPRM1 · rs1799971
See detailed info →Showing 20 of 9061 · page 453 of 454
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.