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Standard

Sex hormone-binding globulin levels

CUX2 · rs16941230

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−27, with 3 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 310,323 European ancestry individuals, 5,523 African ancestry individuals, 6,638 South Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0735 higher (95% confidence interval 0.06-0.087); p = 2 × 10−27.

Where it sits Chromosome 12, band 12q24.11 — in an intron of CUX2.

How common each version is

AC
Korean KRGDB
A 99.7% · C 0.3%
Korean Korea4K
A 99.6% · C 0.4%
Korean Korea1K
A 99.7% · C 0.3%
Japanese ToMMo
A 99.9% · C 0.1%
Vietnamese
A 98.1% · C 1.9%
World gnomAD
A 96.0% · C 4.0%
World 1000 Genomes
A 96.3% · C 3.7%
World TOPMed
A 96.1% · C 3.9%

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.

What each result means

A/A No copy of the version the research linked to Sex hormone-binding globulin levels. This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Sex hormone-binding globulin levels. That is a smaller link than two copies.
C/C Two copies of the version the research linked to Sex hormone-binding globulin 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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Sex hormone-binding globulin levels (rs16941230). MyGeneLog™. https://www.mygenelog.com/variants/rs16941230

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