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Standard

HDL cholesterol

MBNL1 · rs3773910

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−10, 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 215,551 European ancestry individuals, 57,332 African American individuals, 24,743 Hispanic individuals; replicated in Up to 319,677 individuals.

The effect Each copy of the C allele shifted the measure 0.0161 mg dl-1 lower (95% confidence interval 0.011-0.021); p = 1 × 10−10.

How common The C allele had a frequency of about 76% in the people studied.

Where it sits Chromosome 3, band 3q25.2 — in an intron of MBNL1.

How common each version is

CG
Korean KRGDB
C 73.7% · G 26.4%
Korean Korea4K
C 74.7% · G 25.3%
Korean Korea1K
C 74.0% · G 26.0%
Japanese ToMMo
C 77.2% · G 22.8%
Vietnamese
C 82.5% · G 17.4%
World gnomAD
C 78.1% · G 21.9%
World 1000 Genomes
C 78.0% · G 22.0%
World TOPMed
C 77.5% · G 22.4%

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

C/C Two copies of the version the research linked to HDL cholesterol. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/G One copy of the version the research linked to HDL cholesterol. That is a smaller link than two copies.
G/G No copy of the version the research linked to HDL cholesterol. This is the starting point the study compared everyone against.
Source

Quoting this page

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HDL cholesterol (rs3773910). MyGeneLog™. https://www.mygenelog.com/variants/rs3773910

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