Standard

End-diastolic bi-ventricular shape (principal component 9)

near SLC35F1 · rs56403768

What the study found

Who was studied 35,055 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.049 lower (95% confidence interval 0.035-0.063); p = 7 × 10−12.

How common The T allele had a frequency of about 42% in the people studied.

Where it sits Chromosome 6, band 6q22.31 — between genes, 64.7 kb from SLC35F1.

What each result means

C/C No copy of the version the research linked to End-diastolic bi-ventricular shape (principal component 9). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to End-diastolic bi-ventricular shape (principal component 9). That is a smaller link than two copies.
T/T Two copies of the version the research linked to End-diastolic bi-ventricular shape (principal component 9). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs56403768

What is rs56403768?

rs56403768 is a single position in the genome, in or near the near SLC35F1 gene. Published research associates it with end-diastolic bi-ventricular shape (principal component 9). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs56403768 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 rs56403768 come from?

GWAS Catalog, Nature communications 2024, PMID:39543113. 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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End-diastolic bi-ventricular shape (principal component 9) (rs56403768). MyGeneLog™. https://www.mygenelog.com/variants/rs56403768

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