Variants linked to Kidney Function

Continuously updated · newest added Oct 25, 2026

342 positions on this site are linked to Kidney Function, out of 118,864 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

Estimated glomerular filtration rate

CELF1 · rs11039221

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Standard

Estimated glomerular filtration rate

C2orf73 · rs17046036

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Standard

Estimated glomerular filtration rate

MKL1 · rs17001943

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Standard

Estimated glomerular filtration rate

GAB2 · rs2063724

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Standard

Urinary albumin excretion (no hypertensive medication)

C15orf48 · rs16943246

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Standard

Urinary albumin excretion (no hypertensive medication)

CHD7 · rs4738817

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Standard

Urinary albumin excretion (no hypertensive medication)

CPO · rs6712846

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Standard

Estimated glomerular filtration rate

SLC47A1 · rs2440164

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Standard

Estimated glomerular filtration rate

PHTF2 · rs10270542

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Standard

Estimated glomerular filtration rate

FAM122A · rs2039424

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Standard

Estimated glomerular filtration rate

PRKAG2 · rs6464165

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Standard

Estimated glomerular filtration rate

GFRAL · rs143297173

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Standard

Estimated glomerular filtration rate

RPS10 · rs28847046

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Sensitive

Fractional excretion of metabolites in chronic kidney disease

LOC284294 · rs11662622

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Standard

Glomerular filtration rate (creatinine)

LPHN2 · rs10874312

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Standard

Creatinine levels

SLC34A1 · rs3812036

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Standard

Glomerular filtration rate

LRP2 · rs57989581

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Standard

Glomerular filtration rate

NFATC1 · rs8096658

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Standard

Glomerular filtration rate

TFDP2 · rs1511299

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Standard

Glomerular filtration rate in non diabetics (creatinine)

A1CF · rs10994860

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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.