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Standard

A body shape index

HLA-B · rs2257269

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, 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 219,872 British ancestry women.

The effect Each copy of the A allele shifted the measure 0.0159 higher (95% confidence interval 0.01-0.022); p = 3 × 10−8.

Where it sits Chromosome 6, band 6p21.33 — a synonymous change in HLA-B.

How common each version is

AG
Korean KRGDB
A 35.9% · G 64.1%
Japanese ToMMo
A 18.1% · G 81.9%
World gnomAD
A 15.6% · G 84.4%
World 1000 Genomes
A 40.0% · G 60.0%

By ancestry gnomAD

East Asian
A 10.1% · G 89.9%
European (non-Finnish)
A 17.7% · G 82.3%
African / African American
A 12.0% · G 88.0%
South Asian
A 8.5% · G 91.5%
Admixed American (Latino)
A 16.7% · G 83.3%
Middle Eastern
A 19.6% · G 80.4%
Finnish
A 8.9% · G 91.1%
Ashkenazi Jewish
A 32.8% · G 67.2%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study. The ancestry rows are gnomAD's own groups (via Ensembl), as the survey defines them, not races.

What each result means

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

Quoting this page

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A body shape index (rs2257269). MyGeneLog™. https://www.mygenelog.com/variants/rs2257269

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