Sensitive

Breast cancer

SLC4A7 · rs4973768

Where this position leads

Condition: Breast Cancer

rs4973768 Condition: Breast Cancer Breast Cancer Condition rs4973768 rs4973768 SLC4A7

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Breast cancer compared to the general population. (GWAS Catalog, J Natl Cancer Inst 2011, PMID:21263130)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Breast cancer. (GWAS Catalog, J Natl Cancer Inst 2011, PMID:21263130)
T/T Published research associates this genotype with typical/baseline likelihood of Breast cancer — no copies of the reported risk allele. (GWAS Catalog, J Natl Cancer Inst 2011, PMID:21263130)

Source: GWAS Catalog, J Natl Cancer Inst 2011, PMID:21263130

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs4973768

What is rs4973768?

rs4973768 is a single position in the genome, in or near the SLC4A7 gene. Published research associates it with breast cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs4973768 linked to?

On MyGeneLog this position is linked to Breast Cancer. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs4973768?

Subjects that appear in the title or abstract of the same papers as this rsID include alcohol and the flush (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs4973768 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs4973768 come from?

GWAS Catalog, J Natl Cancer Inst 2011, PMID:21263130. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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