Variants linked to C-Reactive Protein Levels

Continuously updated · newest added Oct 23, 2026

646 positions on this site are linked to C-Reactive Protein Levels, out of 110,343 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 C-Reactive Protein Levels

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C-reactive protein levels (MTAG)

DPF3 · rs8006178

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C-reactive protein levels (UKB data field 30710)

near C12orf43 · rs189396052

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C-reactive protein levels

ATP8B2 · rs41310887

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C-reactive protein levels (UKB data field 30710)

near CRP · rs146797155

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C-reactive protein levels

near BAAT · rs11790458

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C-reactive protein levels

GLUD1P3 · rs11000760

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C-reactive protein levels (UKB data field 30710)

HNF1A-AS1 · rs192127960

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C-reactive protein levels

AK4 · rs142603322

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C-reactive protein levels (MTAG)

SEMA3F · rs75208336

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C-reactive protein levels

RAB37 · rs6501734

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C-reactive protein levels

RGS17 · rs1338071

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C-reactive protein levels

ATP8B2 · rs77993403

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C-reactive protein levels

near IL1RN · rs315946

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C-reactive protein levels

near DUSP23 · rs181704186

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C-reactive protein levels

CRP · rs149520992

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C-reactive protein levels

near PDE4B · rs116643857

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C-reactive protein levels

LINC01705 · rs11577023

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C-reactive protein levels (MTAG)

near ATG16L2 · rs10898880

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C-reactive protein levels (UKB data field 30710)

CABP1 · rs148446759

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C-reactive protein levels (UKB data field 30710)

OASL · rs140478455

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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.