Gene Knowledge Graph
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Variants linked to Monocyte Count

Continuously updated · newest added Nov 7, 2026

634 positions on this site are linked to Monocyte Count, out of 2,505,098 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 RPL31P10 · rs4020660

See detailed info → Standard

Monocyte count

SPC25 · rs3931

See detailed info → Standard

Monocyte count

DUSP14 · rs865483

See detailed info → Standard

Monocyte count

NFKBIE · rs730775

See detailed info → Standard

Monocyte count

ADCY5 · rs17295246

See detailed info → Standard

Monocyte count

RP11-419K12.1 · rs6993442

See detailed info → Standard

Monocyte count

EHD3 · rs184409696

See detailed info → Standard

Monocyte count

GYPA · rs4240356

See detailed info → Standard

Monocyte count

ARRDC2 · rs35928002

See detailed info → Standard

Monocyte count

ADO · rs224082

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Monocyte count

near CXCR4 · rs13022141

See detailed info → Standard

Monocyte count

MIR142 · rs2632516

See detailed info → Standard

Monocyte count

SH2B3 · rs540639423

See detailed info → Standard

Monocyte count

PLAGL1 · rs149110519

See detailed info → Standard

Monocyte count

VARS · rs9469054

See detailed info → Standard

Monocyte count

FAM46C · rs1370297

See detailed info → Standard

Monocyte count (UKB data field 30130)

near UQCRHP1 · rs62395789

See detailed info → Standard

Monocyte count

IL6R · rs4393147

See detailed info → Standard

Monocyte count

MIR3667HG · rs763127

See detailed info → Standard

Monocyte count (UKB data field 30130)

LRRC8B · rs12733491

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Showing 20 of 634 · page 6 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.