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Standard

Childhood body mass index

near LINGO2 · rs10968118

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−10, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 441,761 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0135 lower (95% confidence interval 0.0094-0.0176); p = 1 × 10−10.

Where it sits Chromosome 9, band 9p21.2 — between genes, 134.6 kb from LINGO2.

What each result means

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

Quoting this page

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Childhood body mass index (rs10968118). MyGeneLog™. https://www.mygenelog.com/variants/rs10968118

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