Variants linked to Monocyte Count

Continuously updated · newest added Oct 26, 2026

525 positions on this site are linked to Monocyte Count, out of 272,464 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 MIR7702 · rs28430334

See detailed info →
Standard

Monocyte count

near IRF8 · rs72805168

See detailed info →
Standard

Monocyte count

SSH2 · rs2729450

See detailed info →
Standard

Monocyte count

near UBASH3B · rs11600178

See detailed info →
Standard

Monocyte count

RP11-542M13.3 · rs12711490

See detailed info →
Standard

Monocyte count

EHD4 · rs1002774

See detailed info →
Standard

Monocyte count

DHFRP2 · rs2523552

See detailed info →
Standard

Monocyte count

RP11-202G18.1 · rs12339013

See detailed info →
Standard

Monocyte count

RPN1 · rs6789546

See detailed info →
Standard

Monocyte count

CCDC26 · rs10092988

See detailed info →
Standard

Monocyte count

PAN3 · rs145096717

See detailed info →
Standard

Monocyte count

SSH2 · rs880749

See detailed info →
Standard

Monocyte count

CCND3 · rs142449754

See detailed info →
Standard

Monocyte count

SCD5 · rs6824723

See detailed info →
Standard

Monocyte count

near LINC01565 · rs4045811

See detailed info →
Standard

Monocyte count

CCDC26 · rs35389394

See detailed info →
Standard

Monocyte count

near UBASH3B · rs7121365

See detailed info →
Standard

Monocyte count

PRTFDC1 · rs112955547

See detailed info →
Standard

Monocyte count

HLA-B · rs2523562

See detailed info →
Standard

Monocyte count

CSF1R · rs6874087

See detailed info →

Showing 20 of 525 · page 1 of 27

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.