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Standard

Blood urea nitrogen (BUN, maximum, inv-norm transformed)

near RAPSN · rs77998085

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−19, 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 117,530 African American or Afro-Caribbean individuals, 57,007 Hispanic or Latin American individuals, 6,277 East Asian ancestry individuals, 418,135 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0264 higher (95% confidence interval 0.021-0.032); p = 1 × 10−19.

How common The C allele had a frequency of about 82% in the people studied.

Where it sits Chromosome 11, band 11p11.2 — between genes, 5.1 kb from RAPSN.

How common each version is

CT
Korean KRGDB
C 60.3% · T 39.7%
Korean Korea4K
C 60.5% · T 39.5%
Korean Korea1K
C 61.5% · T 38.5%
Japanese ToMMo
C 58.3% · T 41.7%
World gnomAD
C 79.0% · T 21.0%
World 1000 Genomes
C 76.6% · T 23.4%
World TOPMed
C 78.5% · T 21.5%

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 Blood urea nitrogen (BUN, maximum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Blood urea nitrogen (BUN, maximum, inv-norm transformed). That is a smaller link than two copies.
T/T No copy of the version the research linked to Blood urea nitrogen (BUN, maximum, inv-norm transformed). This is the starting point the study compared everyone against.
Source

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Blood urea nitrogen (BUN, maximum, inv-norm transformed) (rs77998085). MyGeneLog™. https://www.mygenelog.com/variants/rs77998085

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