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vWF levels

DAB2IP · rs10985344

What the study found

Who was studied 42,379 European ancestry individuals, 3,700 African American individuals, 275 Hispanic individuals.

The effect Each copy of the A allele shifted the measure 0.017 higher (95% confidence interval 0.011-0.023); p = 3 × 10−9.

How common The A allele had a frequency of about 25% in the people studied.

Where it sits Chromosome 9, band 9q33.2 — in an intron of DAB2IP.

What each result means

A/A Two copies of the version the research linked to vWF levels. 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 vWF levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to vWF levels. This is the starting point the study compared everyone against.
Source

Questions about rs10985344

What is rs10985344?

rs10985344 is a single position in the genome, in or near the DAB2IP gene. Published research associates it with vwf levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10985344 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 rs10985344 come from?

GWAS Catalog, Circulation 2019, PMID:30586737. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

vWF levels (rs10985344). MyGeneLog™. https://www.mygenelog.com/variants/rs10985344

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