Variants linked to C-Reactive Protein Levels

Continuously updated · newest added Oct 23, 2026

648 positions on this site are linked to C-Reactive Protein Levels, out of 110,847 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)

near UNGP1 · rs150044976

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C-reactive protein levels (UKB data field 30710)

LEPR · rs80343559

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C-reactive protein levels

SNAPC4 · rs78428995

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C-reactive protein levels (UKB data field 30710)

P2RX7 · rs61953400

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C-reactive protein levels

CAMKV · rs2681780

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C-reactive protein levels

PDE4B · rs72679119

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C-reactive protein levels (MTAG)

ERI1 · rs4841101

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C-reactive protein levels (MTAG)

OASL · rs139868663

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C-reactive protein levels (UKB data field 30710)

LINC02819 · rs140891975

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C-reactive protein levels (UKB data field 30710)

near CRPP1 · rs188278364

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High-sensitivity C-reactive protein levels

LNCOB1 · rs148665049

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C-reactive protein levels (MTAG)

OASL · rs76102919

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C-reactive protein levels (MTAG)

ADCY3 · rs6545790

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C-reactive protein levels (MTAG)

GATC · rs117976328

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C-reactive protein levels (MTAG)

SPPL3 · rs117816983

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C-reactive protein levels

near RNU6-1088P · rs11065079

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C-reactive protein levels (MTAG)

CABP1 · rs73222792

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High-sensitivity C-reactive protein levels in HIV infection

CRP · rs6667499

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C-reactive protein levels (MTAG)

near LEPR · rs58846684

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C-reactive protein levels (MTAG)

HNF1A-AS1 · rs141131173

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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.