Variants linked to Nephrotic Syndrome without Mention of Glomerulonephritis

Continuously updated · newest added Oct 21, 2026

12 positions on this site are linked to Nephrotic Syndrome without Mention of Glomerulonephritis, out of 103,358 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Nephrotic Syndrome without Mention of Glomerulonephritis

Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

near SCYGR5 · rs191924967

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

near UNC93B5 · rs555013895

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

near PDIA4 · rs572850354

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

SLC6A18 · rs529814603

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

SFMBT2 · rs190692818

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

near ZNF469 · rs118076421

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

SEMA3E · rs143538480

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

LIMA1 · rs538515780

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

near LINC02740 · rs534357542

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

DOCK8 · rs190789398

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

ARID3B · rs188468626

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Sensitive

Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2)

near LINC02443 · rs184305217

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Questions about variants on this site

What is a "variant" page on this site?

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.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

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.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.