Variants linked to Breast Cancer

Continuously updated · newest added Oct 22, 2026

233 positions on this site are linked to Breast Cancer, out of 108,158 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

LINC00536 · rs13267382

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Sensitive

Breast cancer

near CBX8 · rs745570

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Sensitive

Breast cancer (estrogen-receptor negative)

ANKLE1 · rs67397200

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Sensitive

Breast cancer (estrogen-receptor negative)

KLF5 · rs6562760

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Sensitive

Breast cancer (estrogen-receptor negative)

near ZNF365 · rs10995201

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Sensitive

Breast cancer (estrogen-receptor negative)

near CCDC170 · rs9397437

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Sensitive

Breast cancer (estrogen-receptor negative)

LGR6 · rs6678914

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Sensitive

Breast cancer

SUB1 · rs2012709

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Sensitive

Breast cancer

EXO1 · rs72755295

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Sensitive

Breast cancer

OTUD7B · rs12048493

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Sensitive

Plasma estrone conjugates levels in resected early stage estrogen-receptor positive breast cancer

SLCO1B1 · rs2900478

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Sensitive

Breast cancer

LMO4 · rs12118297

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Sensitive

Breast cancer

LINC00160 · rs16992204

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Sensitive

Breast cancer

FGFR2 · rs2981582

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Sensitive

Breast cancer (estrogen-receptor positive)

near TNP1 · rs12998806

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Sensitive

Response to tamoxifen in breast cancer

C10orf11 · rs10509373

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Sensitive

Breast cancer

DNAJC1 · rs11814448

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Sensitive

Breast cancer

PRC1 · rs2290203

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Sensitive

Breast cancer

ZC3H11A · rs4951011

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Sensitive

Breast cancer

ARRDC3 · rs10474352

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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.