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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.

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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 (UKB data field 30130)

BMP2K · rs2288254

See detailed info → Standard

Monocyte count

near MIR17HG · rs76115890

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Monocyte count

near MVK · rs7314538

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Monocyte count (UKB data field 30130)

LINC01934 · rs115145822

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Monocyte count (UKB data field 30130)

near C1GALT1P1 · rs10878961

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Monocyte count (UKB data field 30130)

NREP · rs6888574

See detailed info → Standard

Monocyte count

RP1-27K12.2 · rs632497

See detailed info → Standard

Monocyte count

RP4-684O24.5 · rs6045639

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Monocyte count

near RNF216 · rs4720652

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Monocyte count

BCAS3 · rs191380121

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Monocyte count (UKB data field 30130)

HIVEP3 · rs1886729

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Monocyte count

AHR · rs17700436

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Monocyte count

near RAB7A · rs146667422

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Monocyte count

near RN7SL222P · rs12363256

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Monocyte count

ZBTB16 · rs1184748

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Monocyte count (UKB data field 30130)

ATRN · rs1064833

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Monocyte count (UKB data field 30130)

SIK3 · rs78692246

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Monocyte count (UKB data field 30130)

PTGR1 · rs72748059

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Monocyte count

PILRA · rs6965458

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Monocyte count (UKB data field 30130)

IPMK · rs61873883

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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.