Variants linked to Hodgkin Lymphoma

Continuously updated · newest added Oct 19, 2026

37 positions on this site are linked to Hodgkin Lymphoma, out of 97,276 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

Malignant lymphoma (Non-Hodgkin lymphoma, multiple myeloma, or Hodgkin lymphoma)

POLR1HASP · rs9258807

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Standard

Hodgkin's lymphoma

C19orf57 · rs77270337

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Standard

Hodgkin's lymphoma

ZNF823 · rs200560875

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Standard

Hodgkin's lymphoma

MAGEC1 · rs41299076

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Standard

Hodgkin's lymphoma

ACE · rs372565955

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Standard

Hodgkin's lymphoma

ATP13A5 and ATP13A5-AS1 · rs78188075

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Standard

Hodgkin's lymphoma

KIF16B · rs2236145

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Standard

Hodgkin's lymphoma

TEX55 and IGSF11 · rs149982219

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Standard

Hodgkin's lymphoma

SERPINF2 · rs141696263

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Standard

Hodgkin's lymphoma

SHANK2 · rs201642016

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Sensitive

Hodgkin's disease (PheCode 201)

near SHMT1 · rs181755438

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Standard

Hodgkin's lymphoma

ESYT3 · rs191240658

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Standard

Hodgkin's lymphoma

TMEM169 · rs140150309

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Standard

Hodgkin's lymphoma

CDCP2 · rs138864964

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Sensitive

Hodgkin's disease (PheCode 201)

GALNTL5 · rs576160676

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Standard

Hodgkin's lymphoma

PGRMC1 · rs145582672

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Sensitive

Hodgkin's disease (PheCode 201)

NFIX · rs1047391271

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Sensitive

Hodgkin's disease (PheCode 201)

near LPAR1 · rs547573644

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Standard

Hodgkin's lymphoma

CPLANE1 · rs200612080

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Sensitive

Hodgkin's disease (PheCode 201)

RNF141 · rs377333979

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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.