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 2,505,673 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

← Back to Monocyte Count

Monocyte count (UKB data field 30130)

EEFSEC · rs61740550

See detailed info → Standard

Monocyte count (UKB data field 30130)

near RPN1 · rs568928278

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Monocyte count

IRF8 · rs182056137

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Monocyte count

POU2F2 · rs79871448

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Monocyte count

XXbac-BPG299F13.17 · rs7741829

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Monocyte count

LINC01755 · rs7547019

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Monocyte count (UKB data field 30130)

near ACER1 · rs4807860

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Monocyte count (UKB data field 30130)

ADCY9 · rs2601823

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Monocyte count (UKB data field 30130)

CERKL · rs17305807

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Monocyte count

CSNK1G1 · rs8033972

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Monocyte count

RUNX2 · rs77182156

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Monocyte count (UKB data field 30130)

LINC02458 · rs2126606

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Monocyte count

APLF · rs190855339

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Monocyte count (UKB data field 30130)

ACAD9 · rs184937941

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Monocyte count (UKB data field 30130)

LINC01934 · rs184413078

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Monocyte count

near LINC01934 · rs115583150

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Monocyte count (UKB data field 30130)

RUNX1 · rs11088296

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Monocyte count

near LINC02132 · rs12596402

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Monocyte count (UKB data field 30130)

HCG27 · rs17197658

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Monocyte count

near CYP4F44P · rs145097765

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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.