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

near RNY1P8 · rs12870942

See detailed info →
Sensitive

Breast cancer

near RPS15P4 · rs11680449

See detailed info →
Sensitive

Breast cancer

C2CD6 · rs77688320

See detailed info →
Sensitive

Chronotype and breast cancer

near CASC16 · rs4608329

See detailed info →
Sensitive

Uterine leiomyoma or breast cancer (pleiotropy)

GSTM2 · rs4147562

See detailed info →
Sensitive

Breast cancer, ovarian cancer or prostate cancer (pleiotropy)

INCENP · rs7937840

See detailed info →
Sensitive

Breast cancer

CASC15 · rs7760611

See detailed info →
Sensitive

Uterine leiomyoma or ER positive breast cancer (pleiotropy)

TESHL · rs77549302

See detailed info →
Sensitive

Breast cancer

near Y_RNA · rs6752414

See detailed info →
Sensitive

Breast cancer

near EGR2 · rs61865900

See detailed info →
Sensitive

Breast cancer

TACC2 · rs2253762

See detailed info →
Sensitive

Breast cancer

near Y_RNA · rs141447235

See detailed info →
Sensitive

Breast cancer

CD9 · rs114003206

See detailed info →
Sensitive

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

C11orf65 · rs10890841

See detailed info →
Sensitive

Breast cancer

FILIP1L · rs9837602

See detailed info →
Sensitive

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

NR2F6 · rs77825513

See detailed info →
Sensitive

Chronotype and breast cancer

near MDFIC · rs62467945

See detailed info →
Sensitive

BRCA1 mutation in breast cancer

JUP · rs9901834

See detailed info →
Sensitive

Breast cancer

near EMB · rs72749841

See detailed info →
Sensitive

Breast cancer

HNF4G · rs189268208

See detailed info →

Showing 20 of 232 · page 2 of 12

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.