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 2,505,478 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 HLA-DOA · rs35520555

See detailed info → Standard

Monocyte count

ADGRV1 · rs73187156

See detailed info → Standard

Monocyte count

IL12A-AS1 · rs66538855

See detailed info → Standard

Monocyte count

near MIR148A · rs60575314

See detailed info → Standard

Monocyte count

LINC01478 · rs144171632

See detailed info → Standard

Monocyte count

MIR4435-2HG · rs76649092

See detailed info → Standard

Monocyte count

near BCL2A1 · rs62025494

See detailed info → Standard

Monocyte count

near APOBEC3H · rs113023

See detailed info → Standard

Monocyte count

ENG · rs41492548

See detailed info → Standard

Monocyte count

TCF3 · rs740436

See detailed info → Standard

Monocyte count

RP11-33B1.2 · rs9307475

See detailed info → Standard

Monocyte count

PRKCE · rs2595205

See detailed info → Standard

Monocyte count

near MIR148A · rs2391170

See detailed info → Standard

Monocyte count variance

VAV1 · rs147731320

See detailed info → Standard

Monocyte count

LINC02768 · rs10927116

See detailed info → Standard

Monocyte count

PARVB · rs10483221

See detailed info → Standard

Monocyte count

RIN3 · rs147042536

See detailed info → Standard

Monocyte count

near CYRIA · rs1430058

See detailed info → Standard

Monocyte count

IL17RA · rs141573482

See detailed info → Standard

Monocyte count

ARID4B · rs12402243

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Showing 20 of 634 · page 15 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.