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Standard

High density lipoprotein cholesterol levels

ABCA1 · rs2740488

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−52, with 437 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.

How common each version is

AC
Korean KRGDB
A 74.2% · C 25.8%
Korean Korea4K
A 75.6% · C 24.4%
Korean Korea1K
A 74.7% · C 25.3%
Japanese ToMMo
A 71.6% · C 28.4%
World gnomAD
A 70.7% · C 29.3%
World 1000 Genomes
A 67.4% · C 32.6%
World TOPMed
A 69.4% · C 30.6%

By ancestry gnomAD

East Asian
A 75.8% · C 24.2%
European (non-Finnish)
A 73.8% · C 26.2%
African / African American
A 61.9% · C 38.1%
South Asian
A 65.7% · C 34.3%
Admixed American (Latino)
A 71.9% · C 28.1%
Middle Eastern
A 69.0% · C 30.9%
Finnish
A 81.8% · C 18.2%
Ashkenazi Jewish
A 75.1% · C 24.9%

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

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

Quoting this page

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High density lipoprotein cholesterol levels (rs2740488). MyGeneLog™. https://www.mygenelog.com/variants/rs2740488

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