Variants linked to Chronic Glomerulonephritis, NOS

Continuously updated · newest added Oct 21, 2026

16 positions on this site are linked to Chronic Glomerulonephritis, NOS, out of 103,022 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 Chronic Glomerulonephritis, NOS

Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

RPS6KA5 · rs76750653

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

CACNA1C · rs546344752

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near RNA5SP169 · rs150253734

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

COL4A4 · rs148222753

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near ADIPOQ · rs113318568

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

GPC6 · rs529136267

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

CDH19 · rs182059755

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

PRKN · rs183510019

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near DNAJB6 · rs557661665

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

ADGRL2 · rs180843162

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near RNA5SP199 · rs189830598

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near LINC02947 · rs192056986

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

CDK14 · rs116915466

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near GPCPD1 · rs551919440

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

PEX10 · rs529217596

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Standard

Chronic glomerulonephritis, NOS (PheCode 580.14)

near MIR3201 · rs185537078

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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.