Variants linked to Kidney Function

Continuously updated · newest added Oct 25, 2026

342 positions on this site are linked to Kidney Function, out of 118,630 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 Kidney Function

Standard

Glomerular filtration rate (creatinine)

TSPAN9 · rs10491967

See detailed info →
Standard

Glomerular filtration rate (creatinine)

NFKB1 · rs228611

See detailed info →
Standard

Glomerular filtration rate (creatinine)

KBTBD2 · rs3750082

See detailed info →
Standard

Glomerular filtration rate (creatinine)

WNT7A · rs6795744

See detailed info →
Standard

Glomerular filtration rate (creatinine)

SIPA1L3 · rs11666497

See detailed info →
Sensitive

Chronic kidney disease

PRKAG2 · rs7805747

See detailed info →
Sensitive

Chronic kidney disease

SLC6A13 · rs10774021

See detailed info →
Sensitive

Chronic kidney disease

SETDB1 · rs267734

See detailed info →
Sensitive

Chronic kidney disease

PHTF2 · rs6465825

See detailed info →
Standard

Urinary albumin excretion

FOXD2 · rs10157710

See detailed info →
Standard

Urinary albumin excretion

PHC2 · rs12032996

See detailed info →
Standard

Urinary albumin excretion

FUT1 · rs838142

See detailed info →
Standard

Urinary albumin excretion

FBXL20 · rs2338796

See detailed info →
Standard

Urinary albumin excretion

AQP7 · rs144994089

See detailed info →
Standard

Urinary albumin excretion

ADO · rs10995311

See detailed info →
Standard

Urinary albumin excretion

CUBN · rs141640975

See detailed info →
Standard

Urinary albumin excretion

COL4A4 · rs35483183

See detailed info →
Standard

Urinary albumin excretion

SBF2 · rs17368443

See detailed info →
Standard

Urinary albumin excretion

CUBN · rs144360241

See detailed info →
Standard

Urinary albumin excretion

SPHKAP · rs35924503

See detailed info →

Showing 20 of 342 · page 16 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.