Gene Knowledge Graph
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Variants linked to Monocyte Count

Continuously updated · newest added Nov 8, 2026

634 positions on this site are linked to Monocyte Count, out of 2,505,333 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Monocyte Count

Standard

Monocyte count

near CITED4 · rs41268099

See detailed info → Standard

Monocyte count

ITGA4 · rs13029144

See detailed info → Standard

Monocyte count

NOS1AP · rs60441301

See detailed info → Standard

Monocyte count

IFITM2 · rs3809112

See detailed info → Standard

Monocyte count

TENT5C · rs67224956

See detailed info → Standard

Monocyte count

IKZF1 · rs62447197

See detailed info → Standard

Monocyte count

VMP1 · rs2777895

See detailed info → Standard

Monocyte count

IRF8 · rs16939945

See detailed info → Standard

Monocyte count

EHD4 · rs4286082

See detailed info → Standard

Monocyte count

C20orf112 · rs1555133

See detailed info → Standard

Monocyte count

ST20 · rs184575290

See detailed info → Standard

Monocyte count

FIRRM · rs4987353

See detailed info → Standard

Monocyte count variance

FLT3 · rs79490353

See detailed info → Standard

Monocyte count

near CRYBG2 · rs7416513

See detailed info → Standard

Monocyte count

DOCK10 · rs6436515

See detailed info → Standard

Monocyte count

ACOXL · rs3789087

See detailed info → Standard

Monocyte count

RREB1 · rs557074

See detailed info → Standard

Monocyte count

TSPO · rs138918

See detailed info → Standard

Monocyte count

near CXCR4 · rs4954391

See detailed info → Standard

Monocyte count

MGAT4B · rs6883116

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Showing 20 of 634 · page 10 of 32

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.