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Variants linked to Monocyte Count

Continuously updated · newest added Nov 8, 2026

644 positions on this site are linked to Monocyte Count, out of 2,507,191 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

Standard

Monocyte count

near Y_RNA · rs1973325

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Monocyte count

near RPL36AP12 · rs12410168

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Monocyte count

FLT3 · rs9554228

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Monocyte count

TNFRSF1A · rs887477

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Monocyte count

near TSBP1-AS1 · rs9267952

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Monocyte count

AIM1L · rs11247913

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Monocyte count

PIK3CD · rs7516138

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Monocyte count

ARPC2 · rs6736362

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Monocyte count

CMKLR1 · rs10778621

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Monocyte count

RP11-290F20.1 · rs913672

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Monocyte count

RCBTB1 · rs7996207

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Monocyte count

CREB5 · rs10238435

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Monocyte count

near ELOVL6 · rs79375912

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Monocyte count

ARHGAP30 · rs3813609

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Monocyte count

NRIP1 · rs2823002

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Monocyte count

near BEND3 · rs11153046

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Monocyte count

near LINC02132 · rs9933582

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Monocyte count

RP11-576N17.5 · rs4566648

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Monocyte count

near HLA-C · rs9264277

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Monocyte count

KSR1 · rs2948542

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Showing 20 of 644 · page 5 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.