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Who was studied 1,172 Taiwanese Han ancestry cases, 4,688 Taiwanese Han ancestry controls.
The effect
Each copy of the G allele carried 1.37 times the odds of Breast cancer (luminal A) (95% confidence interval 1.25-1.51); p = 5 × 10−11.
How common The G allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 2, band 2p24.1 — in an intron of LDAH.
What each result means
A/ANo copy of the version the research linked to Breast cancer (luminal A). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Breast cancer (luminal A). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Breast cancer (luminal A). That is the strongest link of the three results. A link in a study is not a diagnosis.
Breast cancer research and treatment · 2024 · PMID 37851288
Questions about rs76893106
What is rs76893106?
rs76893106 is a single position in the genome, in or near the LDAH gene. Published research associates it with breast cancer (luminal a). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs76893106 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.
Does having rs76893106 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 rs76893106 come from?
GWAS Catalog, Breast cancer research and treatment 2024, PMID:37851288. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Breast cancer (luminal A) (rs76893106). MyGeneLog™. https://www.mygenelog.com/variants/rs76893106