Variants linked to Breast Cancer

Continuously updated · newest added Oct 22, 2026

232 positions on this site are linked to Breast Cancer, out of 107,852 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 (estrogen-receptor positive)

TESHL · rs16856925

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Sensitive

Uterine leiomyoma or ER negative breast cancer (pleiotropy)

ESR1 · rs851981

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Sensitive

Breast cancer

near ZNF322 · rs71557345

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Sensitive

Cancer code, self-reported: breast cancer (UKB data field 20001_1002)

near MRPS30 · rs182431363

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Sensitive

Breast cancer

near ATE1 · rs12354821

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Sensitive

Chronotype and breast cancer

SLC4A7 · rs115356840

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Sensitive

Breast cancer

SKIDA1 · rs11012730

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Sensitive

Breast cancer or hospitalized COVID-19 (pleiotropy)

TTC28 · rs9620778

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Sensitive

BRCA1 mutation in breast cancer

near RAPSN · rs60882887

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Sensitive

Breast cancer

near ALDH7A1P4 · rs35306388

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Sensitive

Breast cancer

SLC14A2 · rs17743054

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Sensitive

Breast cancer, ovarian cancer or prostate cancer (pleiotropy)

CDKN2A/CDKN2B · rs9657608

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Sensitive

Breast cancer

ZBED6 · rs59867004

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Sensitive

Breast cancer, ovarian cancer or prostate cancer (pleiotropy)

GATAD2A · rs1469713

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Sensitive

Breast cancer

LINC02621 · rs35419901

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Sensitive

Breast cancer subtype (triple negative vs luminal A-like)

near WDR43 · rs7580240

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Sensitive

Breast cancer (luminal A)

LDAH · rs76893106

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Sensitive

Breast cancer

MIER3 · rs11957276

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Sensitive

Uterine leiomyoma or breast cancer (pleiotropy)

near HSPA4 · rs56083805

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Sensitive

Breast cancer, ovarian cancer or prostate cancer (pleiotropy)

MIR1208/PVT1 · rs3802173

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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.