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Body shape phenotype PC2

near BMP6 · rs11243202

What the study found

Who was studied 460,198 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.048 lower (95% confidence interval 0.044-0.052); p = 2 × 10−109.

How common The T allele had a frequency of about 51% in the people studied.

Where it sits Chromosome 6, band 6p24.3 — between genes, 7.2 kb from BMP6.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Body shape phenotype PC2 — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Body shape phenotype PC2.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Body shape phenotype PC2 compared to the general population.
Source

Questions about rs11243202

What is rs11243202?

rs11243202 is a single position in the genome, in or near the near BMP6 gene. Published research associates it with body shape phenotype pc2. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11243202 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 rs11243202 come from?

GWAS Catalog, Science advances 2024, PMID:38640244. 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.

Body shape phenotype PC2 (rs11243202). MyGeneLog™. https://www.mygenelog.com/variants/rs11243202

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