Variants linked to Acquired Hemolytic Anemias

Continuously updated · newest added Oct 18, 2026

10 positions on this site are linked to Acquired Hemolytic Anemias, out of 90,895 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 Acquired Hemolytic Anemias

Standard

Acquired hemolytic anemias (PheCode 283)

near COMMD8 · rs180692929

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Standard

Acquired hemolytic anemias (PheCode 283)

near FOXP4-AS1 · rs76198578

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Standard

Acquired hemolytic anemias (PheCode 283)

near CD300A · rs113372935

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Standard

Acquired hemolytic anemias (PheCode 283)

SBF2 · rs576531990

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Standard

Acquired hemolytic anemias (PheCode 283)

ADGRA2 · rs555460019

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Standard

Acquired hemolytic anemias (PheCode 283)

CNTLN · rs181512541

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Standard

Acquired hemolytic anemias (PheCode 283)

near EQTN · rs192783417

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Standard

Acquired hemolytic anemias (PheCode 283)

ZBTB43 · rs139069715

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Standard

Acquired hemolytic anemias (PheCode 283)

near DMXL1-DT · rs532423545

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Standard

Acquired hemolytic anemias (PheCode 283)

near Y_RNA · rs540777345

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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.