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Body mass index (adult)

MLC1 · rs56330886

What the study found

Who was studied 16,559 African ancestry men, 26,193 African ancestry women; replicated in 2,458 African ancestry men, 7,685 African ancestry women, 152,893 European ancestry men, 171,977 European ancestry women.

The effect Each copy of the G allele shifted the measure 0.093 higher (95% confidence interval 0.062-0.124); p = 3 × 10−9.

How common The G allele had a frequency of about 19% in the people studied.

Where it sits Chromosome 22, band 22q13.33 — in an intron of TTLL8.

What each result means

G/G Two copies of the version the research linked to Body mass index (adult). That is the strongest link of the three results. A link in a study is not a diagnosis.
G/T One copy of the version the research linked to Body mass index (adult). That is a smaller link than two copies.
T/T No copy of the version the research linked to Body mass index (adult). This is the starting point the study compared everyone against.
Source

Questions about rs56330886

What is rs56330886?

rs56330886 is a single position in the genome, in or near the MLC1 gene. Published research associates it with body mass index (adult). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs56330886 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 rs56330886 come from?

GWAS Catalog, PLoS Genet 2017, PMID:28430825. 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 mass index (adult) (rs56330886). MyGeneLog™. https://www.mygenelog.com/variants/rs56330886

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