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 8, 2026

634 positions on this site are linked to Monocyte Count, out of 2,505,333 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 PELATON · rs6125942

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Monocyte count

near MIR4686 · rs72853948

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Monocyte count

RP11-195M16.3 · rs17608459

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Monocyte count

near MIR548G · rs1366691

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Monocyte count

GRM4 · rs150556786

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Monocyte count

near KCNA3 · rs11102143

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Monocyte count

RP11-542M13.3 · rs186454026

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Monocyte count

C1orf132 · rs7522307

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Monocyte count

AHR · rs17643734

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Monocyte count

near LINC02541 · rs2695458

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Monocyte count

LPAR1 · rs7872800

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Monocyte count

GPR156 · rs35902169

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Monocyte count

near KCNJ16 · rs8077619

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Monocyte count

near ZNF608 · rs7704551

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Monocyte count

near CREBL2 · rs10845585

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Monocyte count

GALM-AS1 · rs6544171

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Monocyte count

MEIS1 · rs62144048

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Monocyte count

IL12A-AS1 · rs16831132

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Monocyte count

FANCA · rs72807539

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Monocyte count

MDFIC · rs62470670

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Showing 20 of 634 · page 27 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.