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Brorin levels

VWC2 · rs79731913

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.234 lower (95% confidence interval 0.18-0.28); p = 2 × 10⁻²⁰.

How common The A allele had a frequency of about 94% in the people studied.

Where it sits Chromosome 7, band 7p12.2 — a missense change in VWC2.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Brorin levels compared to the general population.

A/C Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Brorin levels.

C/C Published research associates this genotype with typical/baseline likelihood of Brorin levels — no copies of the reported risk allele.

Source

Mapping the proteo-genomic convergence of human diseases

Pietzner M, Wheeler E, Carrasco-Zanini J, Cortes A, Koprulu M, Wörheide MA, Oerton E, Cook J, Stewart ID, Kerrison ND, Luan J, Raffler J

and 9 more — show all

Arnold M, Arlt W, O'Rahilly S, Kastenmüller G, Gamazon ER, Hingorani AD, Scott RA, Wareham NJ, Langenberg C

Science (New York, N.Y.) · 2021 · PMID 34648354

Questions about rs79731913

What is rs79731913?

rs79731913 is a single position in the genome, in or near the VWC2 gene. Published research associates it with brorin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs79731913 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 rs79731913 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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.

Brorin levels (rs79731913). MyGeneLog™. https://www.mygenelog.com/variants/rs79731913

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