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 2,505,381 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

PM20D1 · rs1772143

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Monocyte count

RP11-543F8.2 · rs2646420

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Monocyte count

near NAT9 · rs895692

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Monocyte count

PM20D1-AS1 · rs9438393

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Monocyte count

CCR2 · rs1799864

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Monocyte count

near PCNPP2 · rs28450540

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Monocyte count

HLA-DPB1 · rs1042133

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Monocyte count

near GSTM5P1 · rs1584063

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Monocyte count

ANKRD55 · rs28722705

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Monocyte count

near U3 · rs186272630

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Monocyte count

near TNFSF13B · rs150861794

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Monocyte count

near RPN1 · rs116026278

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Monocyte count

near RPN1 · rs112097551

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Monocyte count

UQCRC2P1 · rs140058837

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Monocyte count

APOBEC3H · rs60093835

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Monocyte count

NRIP1 · rs7280064

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Monocyte count

near MAFB · rs4812447

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Monocyte count

SIRPB1 · rs34600126

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Monocyte count

BBC3 · rs45474992

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Monocyte count

ERF · rs35493131

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Showing 20 of 634 · page 11 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.