22 positions on this site are linked to Mosaic Loss of Chromosome Y, out of 16,580 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
TCL1A · rs728739
See detailed info → StandardLINC01478 · rs80277818
See detailed info → StandardTCL1A · rs139012944
See detailed info → StandardCDKN1B · rs4251697
See detailed info → StandardFAM117A · rs78997619
See detailed info → StandardCENPN · rs77874075
See detailed info → StandardSENP7 · rs4683900
See detailed info → StandardLOC102724152 · rs4709819
See detailed info → StandardMAD1L1 · rs4721217
See detailed info → StandardNRIP1 · rs117587217
See detailed info → StandardFLT3LG · rs79058858
See detailed info → StandardGPR114 · rs1859259
See detailed info → StandardANGPTL2 · rs138423884
See detailed info → StandardCD164 · rs11251
See detailed info → StandardPSMD13 · rs12225799
See detailed info → StandardZNF423 · rs9921295
See detailed info → StandardKRBA1 · rs55727837
See detailed info → StandardNCAPG2 · rs12668837
See detailed info → StandardZNF462 · rs9299129
See detailed info → StandardTMEM54 · rs527504
See detailed info →Showing 20 of 22 · page 1 of 2
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.