Variants linked to Kidney Function

Continuously updated · newest added Oct 25, 2026

342 positions on this site are linked to Kidney Function, out of 118,504 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Standard

Urinary albumin excretion

AGR3 · rs4410790

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Standard

Urinary albumin excretion

MYL3 · rs6768627

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Standard

Urinary albumin excretion

CWC27 · rs7731168

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Standard

Urinary albumin excretion

WIPF3 · rs17158386

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Standard

Urinary albumin excretion

TRIB1 · rs28601761

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Standard

Urinary albumin excretion

PRKCI · rs112607182

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Standard

Urinary albumin excretion

HOTTIP · rs2023844

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Standard

Urinary albumin excretion

NR3C2 · rs6535594

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Standard

Urinary albumin excretion

SHROOM3 · rs7654754

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Standard

Glomerular filtration rate

SHROOM3 · rs4859682

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Standard

Urinary albumin excretion

LOC730100 · rs6750228

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Standard

Urinary albumin excretion

MIR548AR · rs183131780

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Standard

Urinary albumin excretion

NR5A2 · rs12727980

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Standard

Glomerular filtration rate

SHROOM3 · rs10032549

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Standard

Renal function-related traits (sCR)

UMOD · rs11864909

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Standard

Renal function-related traits (sCR)

WDR72 · rs17730436

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Standard

Creatinine levels

SLC22A2 · rs3127573

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Standard

Renal function-related traits (BUN)

C12orf51 · rs2074356

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Standard

Renal function-related traits (BUN)

DCDC5 · rs10767873

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Sensitive

Renal function and chronic kidney disease

SHROOM3 · rs17319721

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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.