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Standard

Waist circumference adjusted for body mass index

RSPO3 · rs2745353

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−37, with 56 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 up to 56,910 European ancestry men, up to 86,570 European ancestry women; replicated in up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women.

The effect Each copy of the T allele shifted the measure 0.0349 higher (95% confidence interval 0.026-0.044); p = 1 × 10−15.

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

Where it sits Chromosome 6, band 6q22.33 — in an intron of LOC105377989.

How common each version is

CT
Korean KRGDB
C 38.8% · T 61.2%
Korean Korea4K
C 40.8% · T 59.2%
Korean Korea1K
C 39.9% · T 60.1%
Japanese ToMMo
C 41.9% · T 58.1%
Vietnamese
C 42.9% · T 57.1%
World gnomAD
C 45.5% · T 54.5%
World 1000 Genomes
C 44.8% · T 55.2%
World TOPMed
C 44.6% · T 55.4%

By ancestry gnomAD

East Asian
C 40.0% · T 60.0%
European (non-Finnish)
C 48.6% · T 51.4%
African / African American
C 39.2% · T 60.8%
South Asian
C 47.7% · T 52.3%
Admixed American (Latino)
C 45.1% · T 54.9%
Middle Eastern
C 50.7% · T 49.3%
Finnish
C 49.2% · T 50.7%
Ashkenazi Jewish
C 53.9% · T 46.1%

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

C/C No copy of the version the research linked to Waist circumference adjusted for body mass index. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Waist circumference adjusted for body mass index. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Waist circumference adjusted for body mass index. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Quoting this page

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Waist circumference adjusted for body mass index (rs2745353). MyGeneLog™. https://www.mygenelog.com/variants/rs2745353

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