Variants linked to Gout

Continuously updated · newest added Oct 24, 2026

782 positions on this site are linked to Gout, out of 113,825 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 Gout

Standard

Gout

NRXN1-DT · rs147657231

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Standard

Gout

near NALF1 · rs184097678

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Standard

Gout

near PPAT · rs13123542

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Insulin-like growth factor 1 levels

FAM120A · rs78108956

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Standard

Gout

NCOA6 · rs6058108

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Standard

Insulin-like growth factor 1 levels

CMAHP · rs9467442

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Standard

Aspartate aminotransferase to alanine aminotransferase ratio

ARHGAP39 · rs72697668

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Standard

Gout (PheCode 274.1)

near FLJ46284 · rs544648171

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Standard

Aspartate aminotransferase to alanine aminotransferase ratio

NDRG4 · rs17821543

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Standard

Insulin-like growth factor 1 levels

near RPL24P7 · rs12152551

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Standard

Serum phosphate levels

DLEU7 · rs11617827

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Standard

Insulin-like growth factor 1 levels

CBR3-AS1 · rs113596566

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Standard

Insulin-like growth factor 1 levels

PIWIL4-AS1 · rs11020842

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Standard

Insulin-like growth factor 1 levels

BBX · rs9817115

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Standard

Serum phosphate levels

HSPG2 · rs76382135

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Standard

Serum phosphate levels

MAFTRR · rs76075303

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Standard

Insulin-like growth factor 1 levels

near HMGN1P19 · rs73119694

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Vitamin D levels

DOK7 · rs73080940

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Aspartate aminotransferase to alanine aminotransferase ratio

CACNB2 · rs72784221

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Standard

Gout

BRINP3 · rs718609

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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.