Variants linked to C-Reactive Protein Levels

Continuously updated · newest added Oct 23, 2026

640 positions on this site are linked to C-Reactive Protein Levels, out of 109,838 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

Standard

C-reactive protein levels (MTAG)

near CALM2P1 · rs11870969

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Standard

High-sensitivity C-reactive protein levels

near OR10J9P · rs117454944

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Standard

C-reactive protein levels

OR10J8P · rs115368096

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Standard

C-reactive protein levels

NUP210L · rs115178836

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Standard

C-reactive protein

TIMM29 · rs113439314

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Standard

C-reactive protein levels

PPP1R37 · rs113405869

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Standard

C-reactive protein levels (MTAG)

TNKS · rs74822765

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C-reactive protein levels (MTAG)

FDFT1 · rs73207295

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C-reactive protein levels (MTAG)

SKA2 · rs67378767

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C-reactive protein

ERBB4 · rs3791708

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Standard

C-reactive protein levels (MTAG)

near SNHG26 · rs34814028

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C-reactive protein levels (MTAG)

PTPRF · rs2842171

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C-reactive protein levels (MTAG)

HNRNPC · rs12589290

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C-reactive protein levels

BLOC1S3 · rs117783785

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C-reactive protein levels

WWOX · rs34982954

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Standard

C-reactive protein levels (MTAG)

PAX8 · rs77143791

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C-reactive protein levels

SHE · rs139460294

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C-reactive protein levels (MTAG)

PXN · rs117864951

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C-reactive protein levels (MTAG)

PPIEL · rs111452793

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C-reactive protein levels

LEPR · rs77451629

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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.