Sensitive

Renal cell carcinoma

GRB10 · rs73113855

Where this position leads

Condition: Renal Cell Carcinoma

rs73113855 Condition: Renal Cell Carcinoma Renal Cell Carcinoma Condition rs73113855 rs73113855 GRB10

What the study found

Who was studied 5,313 East Asian ancestry cases, 96,912 East Asian ancestry controls, 25,890 European ancestry cases, 743,585 European ancestry controls, 897 African American cases, 3,109 African American controls, 1,612 Hispanic or Latin American cases, 2,180 Hispanic or Latin American controls.

The effect Each copy of the A allele carried 0.87 times the odds of Renal cell carcinoma (95% confidence interval 0.84-0.91); p = 3 × 10−11.

How common The A allele had a frequency of about 10% in the people studied.

Where it sits Chromosome 7, band 7p12.1 — in an intron of GRB10.

What each result means

A/A Two copies of the version the research linked to Renal cell carcinoma. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Renal cell carcinoma. That is a smaller link than two copies.
G/G No copy of the version the research linked to Renal cell carcinoma. This is the starting point the study compared everyone against.
Source

Questions about rs73113855

What is rs73113855?

rs73113855 is a single position in the genome, in or near the GRB10 gene. Published research associates it with renal cell carcinoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs73113855 linked to?

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

Does having rs73113855 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 rs73113855 come from?

GWAS Catalog, Nature communications 2026, PMID:42000752. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Renal cell carcinoma (rs73113855). MyGeneLog™. https://www.mygenelog.com/variants/rs73113855

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