Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license
G6PD · rs1557229683
See detailed info → StandardG6PD · rs2148329890
See detailed info → StandardG6PD · rs200111236
See detailed info → StandardG6PD · rs137852332
See detailed info → StandardG6PD · rs137852336
See detailed info → StandardG6PD · rs2070346788
See detailed info → StandardG6PD · rs137852329
See detailed info → StandardG6PD · rs137852346
See detailed info → StandardG6PD · rs2148330566
See detailed info → StandardG6PD · rs2148328852
See detailed info → SensitiveG6PD · rs1557229736
See detailed info → StandardG6PD · rs2148328873
See detailed info → StandardG6PD · rs137852317
See detailed info → StandardG6PD · rs137852324
See detailed info → StandardG6PD · rs137852322
See detailed info → StandardG6PD · rs1603411177
See detailed info → StandardG6PD · rs387906468
See detailed info → StandardG6PD · rs137852343
See detailed info → StandardG6PD · rs2523261737
See detailed info → StandardG6PD · rs1557229599
See detailed info →Showing 20 of 110 · page 1 of 6
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.