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Variants linked to Monocyte Count

Continuously updated · newest added Nov 8, 2026

636 positions on this site are linked to Monocyte Count, out of 2,505,961 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

F2 · rs3136508

See detailed info → Standard

Monocyte count

BCL2L1 · rs192009275

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Monocyte count

GYPA · rs11723763

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Monocyte count (UKB data field 30130)

KCNN4 · rs74487631

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Monocyte count (UKB data field 30130)

RAB7A · rs137861567

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Monocyte count

CCDC6 · rs1171819

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Monocyte count

RP11-196G18.3 · rs587626837

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Monocyte count

near CD14 · rs72800905

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Monocyte count

near MIR7702 · rs17227559

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Monocyte count

near CHCHD2P8 · rs112634401

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Monocyte count

near RPL36AP12 · rs9433740

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Monocyte count (UKB data field 30130)

near RN7SL222P · rs7934276

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Monocyte count

CCDC26 · rs74756667

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Monocyte count variance

TMEM121B · rs9605219

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Monocyte count

PREX1 · rs6019386

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Monocyte count

MEF2D · rs3790461

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Monocyte count (UKB data field 30130)

near RNY4P18 · rs369080900

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Monocyte count (UKB data field 30130)

near RNY4P18 · rs184396721

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Monocyte count (UKB data field 30130)

near RPA2 · rs141459612

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Monocyte count (UKB data field 30130)

HECTD4 · rs73207635

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Showing 20 of 636 · page 21 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.