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Standard

High density lipoprotein cholesterol levels

RRN3 · rs11644601

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−457, with 155 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

CT
Korean KRGDB
C 0.0% · T 100.0%
World gnomAD
C 20.4% · T 79.6%
World 1000 Genomes
C 11.4% · T 88.6%
World TOPMed
C 19.3% · T 80.7%

By ancestry gnomAD

East Asian
T 99.8%
European (non-Finnish)
C 29.6% · T 70.4%
African / African American
C 5.3% · T 94.7%
South Asian
C 15.8% · T 84.2%
Admixed American (Latino)
C 19.9% · T 80.1%
Middle Eastern
C 34.0% · T 66.0%
Finnish
C 27.6% · T 72.4%
Ashkenazi Jewish
C 35.3% · T 64.7%

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 High density lipoprotein cholesterol levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to High density lipoprotein cholesterol levels. That is a smaller link than two copies.
T/T 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.
Source

Quoting this page

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High density lipoprotein cholesterol levels (rs11644601). MyGeneLog™. https://www.mygenelog.com/variants/rs11644601

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