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 7, 2026

634 positions on this site are linked to Monocyte Count, out of 2,505,145 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 IKZF1 · rs145532105

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Standard

Monocyte count (UKB data field 30130)

near CDC7 · rs12717798

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Monocyte count

LINC01989 · rs9911144

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Monocyte count

IL17RA · rs879575

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Monocyte count

FLT3 · rs146983744

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Monocyte count (UKB data field 30130)

near MIR7702 · rs55810007

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Standard

Monocyte count (UKB data field 30130)

near ZNF483 · rs200969146

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Monocyte count

VWA7 · rs9461721

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Monocyte count

near LINC00399 · rs9521344

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Monocyte count

ITGA4 · rs155147

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Monocyte count

SLC2A1 · rs17387886

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Monocyte count

near RPL23AP87 · rs9908212

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Monocyte count

RASA2 · rs6800122

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Monocyte count

PAN3 · rs76806311

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Monocyte count

SCD5 · rs6832625

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Monocyte count

near MIR4289 · rs9410380

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Monocyte count

MICB · rs2507971

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Monocyte count

ETS1 · rs34658647

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Monocyte count

NFKB1-AS1 · rs141936164

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Monocyte count

near SPMIP3 · rs61165644

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Showing 20 of 634 · page 9 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.