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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 2,505,478 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

RP11-202G18.1 · rs148166152

See detailed info → Standard

Monocyte count

BAZ1A-AS1 · rs113235072

See detailed info → Standard

Monocyte count

IRF8 · rs13338943

See detailed info → Standard

Monocyte count

LRRC8C-DT · rs2390762

See detailed info → Standard

Monocyte count (UKB data field 30130)

JAZF1-AS1 · rs17156536

See detailed info → Standard

Monocyte count

NREP · rs6869021

See detailed info → Standard

Monocyte count

near RNY4P18 · rs1989183

See detailed info → Standard

Monocyte count

ZYG11A · rs576650

See detailed info → Standard

Monocyte count (UKB data field 30130)

C16orf74 · rs11647718

See detailed info → Standard

Monocyte count

TGFBR3 · rs12735851

See detailed info → Standard

Monocyte count

ITGA4 · rs115713449

See detailed info → Standard

Monocyte count (UKB data field 30130)

CXCR2 · rs3890158

See detailed info → Standard

Monocyte count

HLA-DQA1 · rs28538060

See detailed info → Standard

Monocyte count

LINC02541 · rs1970365

See detailed info → Standard

Monocyte count

near SSBP3 · rs12752990

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Monocyte count (UKB data field 30130)

near LINC02132 · rs11646245

See detailed info → Standard

Monocyte count

near SPMIP3 · rs57203936

See detailed info → Standard

Monocyte count (UKB data field 30130)

PRCPP1 · rs1509497

See detailed info → Standard

Monocyte count

LYST · rs7541057

See detailed info → Standard

Monocyte count (UKB data field 30130)

CXCL12 · rs72790861

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Showing 20 of 634 · page 25 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.