Variants linked to Breast Cancer

Continuously updated · newest added Oct 22, 2026

233 positions on this site are linked to Breast Cancer, out of 108,284 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 Breast Cancer

Sensitive

Breast cancer

AKAP9 · rs6964587

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Sensitive

Breast cancer

CUX1 · rs71559437

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Sensitive

Chronotype and breast cancer

LINC02929 · rs7907439

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Sensitive

Breast cancer

NEK10 · rs11715126

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Sensitive

Breast cancer

LMX1B · rs10760444

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Sensitive

Breast cancer

H19 · rs217727

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Sensitive

Breast cancer

near RNU6-1328P · rs17268829

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Sensitive

Chronotype and breast cancer

near ZNF365 · rs61863443

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Sensitive

Breast cancer

HCN1 · rs55821517

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Sensitive

Breast cancer

PITPNB · rs62235635

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Sensitive

Breast cancer

CCND1 · rs34507830

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Sensitive

Breast cancer

ZMIZ1 · rs1268974

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Sensitive

Breast cancer

ARHGAP27 · rs4763

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Sensitive

Breast cancer

HSPA4 · rs6596100

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Sensitive

Breast cancer

near GNAI2P1 · rs11055888

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Sensitive

Chronotype and breast cancer

TTC28 · rs695459

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Sensitive

Breast cancer

CDKAL1 · rs2223621

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Sensitive

Breast cancer

ANKLE1 · rs56069439

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Sensitive

Breast cancer

EBF1 · rs12332693

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Sensitive

Breast cancer

FGFR2 · rs2912780

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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.