Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Monocyte Count

Continuously updated · newest added Nov 8, 2026

644 positions on this site are linked to Monocyte Count, out of 2,506,953 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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

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Standard

Monocyte count

near MARK3 · rs8006994

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Monocyte count

TNFSF13B · rs374039502

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Monocyte count

near UBASH3B · rs1945392

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Monocyte count

near RRP12 · rs11189154

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Monocyte count

near OR2K2 · rs112219838

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Monocyte count

NKX2-3 · rs11190141

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Monocyte count

CX3CR1 · rs3732378

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Monocyte count

ACOXL · rs150449635

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Monocyte count

AHI1 · rs2614265

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Monocyte count

LRRC8B · rs12118443

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Monocyte count

near RNU7-183P · rs7545591

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Monocyte count

HLA-DOB · rs2071473

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Monocyte count

APOBEC3H · rs11914001

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Monocyte count

near NDUFS5P6 · rs144345073

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Monocyte count

GGT5 · rs28765434

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Monocyte count

near HLA-DRB9 · rs111688133

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Monocyte count

DPP8 · rs660931

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Monocyte count

PACC1 · rs701905

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Monocyte count (UKB data field 30130)

near DUSP14 · rs1016678

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Monocyte count

near RPL36AP12 · rs71660930

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Showing 20 of 644 · page 4 of 33

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.