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Waist-hip ratio

SLC22A3 · rs474513

Where this position leads

Condition: Waist-to-Hip Ratio (Body Fat Distribution)

rs474513 Condition: Waist-to-Hip Ratio (Body Fat Distribution) Waist-to-Hip Ratio (Body Fat Distri… Condition rs474513 rs474513 SLC22A3

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−10, with 2 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 381,152 European female individuals.

The effect Each copy of the A allele shifted the measure 0.0116 higher (95% confidence interval 0.0081-0.0151); p = 7 × 10−11.

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

Where it sits Chromosome 6, band 6q25.3 — in an intron of SLC22A3.

What each result means

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

Questions about rs474513

What is rs474513?

rs474513 is a single position in the genome, in or near the SLC22A3 gene. Published research associates it with waist-hip ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs474513 linked to?

On MyGeneLog this position is linked to Waist-to-Hip Ratio (Body Fat Distribution). The research behind each link, and its sources, are set out on that condition page.

Does having rs474513 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 rs474513 come from?

GWAS Catalog, Human molecular genetics 2019, PMID:30239722. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Waist-hip ratio (rs474513). MyGeneLog™. https://www.mygenelog.com/variants/rs474513

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