Variants linked to Hodgkin Lymphoma

Continuously updated · newest added Oct 20, 2026

37 positions on this site are linked to Hodgkin Lymphoma, out of 97,612 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Hodgkin Lymphoma

Standard

Hodgkin's lymphoma

ZNF526 · rs144433879

See detailed info →
Standard

Hodgkin's lymphoma

CACNA1I · rs58055559

See detailed info →
Sensitive

Hodgkin's disease (PheCode 201)

TTL · rs565643303

See detailed info →
Standard

Hodgkin's lymphoma

DECR2 · rs146760080

See detailed info →
Standard

Hodgkin's lymphoma

MEGF11 · rs150945752

See detailed info →
Sensitive

Hodgkin's disease (PheCode 201)

LINC02737 · rs138809598

See detailed info →
Sensitive

Hodgkin's disease (PheCode 201)

near LINC02838 · rs75229018

See detailed info →
Sensitive

Hodgkin's disease (PheCode 201)

near PLA2G4A · rs532391514

See detailed info →
Sensitive

Hodgkin's disease (PheCode 201)

DRD4 · rs559464313

See detailed info →
Standard

Hodgkin's lymphoma

near COL11A2P1 · rs3129198

See detailed info →
Standard

Hodgkin's lymphoma

near HLA-DQA1 · rs28383311

See detailed info →
Standard

Diffuse large B-cell non-Hodgkin lymphoma

near HLA-DRA · rs138094736

See detailed info →
Standard

Hodgkin's lymphoma

POU2AF1 · rs7111520

See detailed info →
Standard

Hodgkin's lymphoma

OLIG3 · rs1002658

See detailed info →
Standard

Hodgkin's lymphoma

PTPRK · rs9482849

See detailed info →
Standard

Hodgkin's lymphoma

IL13 · rs2069757

See detailed info →
Standard

B cell non-Hodgkin lymphoma

BCL6 · rs6773854

See detailed info →

Showing 17 of 37 · page 2 of 2

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.