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 110,175 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 (UKB data field 30710)

ANAPC5 · rs118176996

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C-reactive protein

FRK · rs1933737

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C-reactive protein levels

CAMKK2 · rs148059420

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C-reactive protein levels (MTAG)

near LINC01571 · rs11860919

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C-reactive protein levels (MTAG)

P2RX7 · rs117692465

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C-reactive protein levels

near P2RX7 · rs75497300

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C-reactive protein levels

KCNN3 · rs55997241

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C-reactive protein levels (CRP.4337.49.2)

near CRPP1 · rs2808628

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C-reactive protein levels (UKB data field 30710)

LINC02819 · rs185990393

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C-reactive protein levels (UKB data field 30710)

HNF1A-AS1 · rs145690965

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C-reactive protein levels (MTAG)

IL6R · rs114879247

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C-reactive protein levels (UKB data field 30710)

near UNGP1 · rs73579967

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C-reactive protein levels (MTAG)

CAMK2G · rs7080350

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C-reactive protein levels (MTAG)

MSRA-DT · rs6987910

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C-reactive protein levels (MTAG)

CENPA · rs34165519

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C-reactive protein levels (UKB data field 30710)

CEACAM22P · rs144908353

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C-reactive protein levels

near MAP4K4 · rs11693537

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C-reactive protein levels (MTAG)

LINC00536 · rs7815807

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C-reactive protein levels

near CBR3-AS1 · rs7280982

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C-reactive protein levels (UKB data field 30710)

near DUSP23 · rs574313745

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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.