Gene Knowledge Graph
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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 2,505,333 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

LYL1 · rs1003393

See detailed info → Standard

Monocyte count

near CLEC4M · rs571497

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Monocyte count

MAPK4 · rs8084255

See detailed info → Standard

Monocyte count

MED24 · rs2302774

See detailed info → Standard

Monocyte count

SMG6 · rs9915112

See detailed info → Standard

Monocyte count

near ITGAL · rs7196129

See detailed info → Standard

Monocyte count

CMKLR1 · rs12312487

See detailed info → Standard

Monocyte count

ETS1 · rs12575164

See detailed info → Standard

Monocyte count

near SESN3 · rs75963851

See detailed info → Standard

Monocyte count

MS4A6E · rs6591578

See detailed info → Standard

Monocyte count

near CXCL12 · rs17482472

See detailed info → Standard

Monocyte count

near PIP5KL1 · rs4836591

See detailed info → Standard

Monocyte count

near NEK6 · rs7863470

See detailed info → Standard

Monocyte count

VLDLR · rs2219143

See detailed info → Standard

Monocyte count

CDX2 · rs1805106

See detailed info → Standard

Monocyte count

IKZF1 · rs78697948

See detailed info → Standard

Monocyte count

GPR116 · rs2012011

See detailed info → Standard

Monocyte count

CCR3 · rs13325613

See detailed info → Standard

Monocyte count

GPR35 · rs34236350

See detailed info → Standard

Monocyte count

AC074391.1 · rs13417564

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Showing 20 of 634 · page 12 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.