Variants linked to Kidney Function

Continuously updated · newest added Oct 25, 2026

342 positions on this site are linked to Kidney Function, out of 118,714 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

Glomerular filtration rate in non diabetics (creatinine)

NFATC1 · rs8091180

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Standard

Glomerular filtration rate in non diabetics (creatinine)

ETV5 · rs10513801

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Standard

Glomerular filtration rate in non diabetics (creatinine)

CACNA1S · rs3850625

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Standard

Glomerular filtration rate in non diabetics (creatinine)

KCNQ1 · rs163160

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Standard

Glomerular filtration rate in non diabetics (creatinine)

INO80 · rs2928148

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Standard

Glomerular filtration rate in non diabetics (creatinine)

CASP9 · rs12124078

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Standard

Glomerular filtration rate

SLC34A1 · rs35716097

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Glomerular filtration rate

UNCX · rs62435145

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Standard

Glomerular filtration rate

SHROOM3 · rs5020545

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Glomerular filtration rate

PDILT · rs77924615

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Glomerular filtration rate (creatinine)

SKIL · rs9682041

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Glomerular filtration rate (creatinine)

UMOD · rs13329952

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Glomerular filtration rate (creatinine)

WDR37 · rs1044261

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Glomerular filtration rate (creatinine)

CDK12 · rs9916302

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Glomerular filtration rate (creatinine)

STC1 · rs3758086

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Glomerular filtration rate (creatinine)

ALMS1 · rs6546838

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Glomerular filtration rate (creatinine)

DAB2 · rs11959928

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Glomerular filtration rate (creatinine)

SLC47A1 · rs2453580

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Standard

Glomerular filtration rate (creatinine)

INO80 · rs476633

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Standard

Glomerular filtration rate (creatinine)

CASP9 · rs1800615

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Showing 20 of 342 · page 15 of 18

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.