10 positions on this site are linked to Childhood Steroid-Sensitive Nephrotic Syndrome, out of 97,738 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
NPHS1 · rs2285450
See detailed info → Sensitivenear HLA-DQB1 · rs9274740
See detailed info → Sensitivenear HLA-DQA1 · rs9271747
See detailed info → Sensitivenear HLA-DQB1 · rs1794497
See detailed info → Sensitivenear HLA-DQB1 · rs2856696
See detailed info → SensitiveCLEC16A · rs8062322
See detailed info → SensitiveNFKBIL1 · rs2857607
See detailed info → SensitiveNPHS1 · rs412175
See detailed info → Sensitivenear CALHM6 · rs2637678
See detailed info → SensitiveHLA-DRB1 · rs28366266
See detailed info →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.