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.

← Back to Kidney Function

Standard

Creatinine levels

FREM2 · rs2197887

See detailed info →
Standard

Creatinine levels

EVC · rs2279252

See detailed info →
Standard

Creatinine levels

ERRFI1 · rs2294889

See detailed info →
Standard

Creatinine levels

SLC8A1 · rs2301343

See detailed info →
Standard

Creatinine levels

GIGYF2 · rs2305137

See detailed info →
Standard

Creatinine levels

EPAS1 · rs2346418

See detailed info →
Standard

Creatinine levels

RBMS1 · rs2357772

See detailed info →
Standard

Creatinine levels

PRORP · rs2415275

See detailed info →
Standard

Creatinine levels

MXI1 · rs2419316

See detailed info →
Standard

Creatinine levels

ABCA1 · rs2437817

See detailed info →
Standard

Creatinine levels

TLK2 · rs2465439

See detailed info →
Standard

Creatinine levels

ARG1 · rs2608914

See detailed info →
Standard

Creatinine levels

ASAP2 · rs2715860

See detailed info →
Standard

Creatinine levels

near GPATCH2 · rs2810779

See detailed info →
Standard

Creatinine levels

near GUCY2D · rs35261002

See detailed info →
Standard

Creatinine levels

near TGFBR3 · rs35973783

See detailed info →
Standard

Creatinine levels

FABP3 · rs35998242

See detailed info →
Standard

Creatinine levels

ARHGAP26 · rs3756374

See detailed info →
Standard

Creatinine levels

CASZ1 · rs3790638

See detailed info →
Standard

Creatinine levels

LRP2 · rs3821129

See detailed info →

Showing 20 of 342 · page 10 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.