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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
1 / 4
Its strongest genetic-study result is p = 10−9, 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 475,645 European ancestry individuals, 8,590 African ancestry individuals, 85,279 East Asian ancestry individuals, 4,270 South Asian ancestry individuals, 14,668 Hispanic or Latin American individuals.
The effect
Each copy of the A allele shifted the measure 6.01 z score higher; p = 2 × 10−9.
How common The A allele had a frequency of about 97% in the people studied.
Where it sits Chromosome 13, band 13q12.3 — in an intron of FLT1.
How common each version is
AG
KoreanKRGDB
A 98.3% · G 1.7%
KoreanKorea4K
A 98.2% · G 1.8%
KoreanKorea1K
A 98.0% · G 2.0%
Japanese ToMMo
A 98.3% · G 1.7%
Vietnamese
A 96.8% · G 3.2%
World gnomAD
A 96.4% · G 3.6%
World 1000 Genomes
A 94.9% · G 5.1%
World TOPMed
A 95.6% · G 4.4%
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.
What each result means
A/ATwo copies of the version the research linked to Lung function (FEV1/FVC). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Lung function (FEV1/FVC). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Lung function (FEV1/FVC). This is the starting point the study compared everyone against.
Nature genetics · 2023 · PMID 36914875 · open access
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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
Lung function (FEV1/FVC) (rs11617354). MyGeneLog™. https://www.mygenelog.com/variants/rs11617354