Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license
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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
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
KoreanKRGDB
C 38.8% · T 61.2%
KoreanKorea4K
C 40.8% · T 59.2%
KoreanKorea1K
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/CNo 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/TOne copy of the version the research linked to Waist circumference adjusted for body mass index. That is a smaller link than two copies.
T/TTwo 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.
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Quoting this page
Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license
Waist circumference adjusted for body mass index (rs2745353). MyGeneLog™. https://www.mygenelog.com/variants/rs2745353