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Standard

Immunoglobulin A vasculitis

near HLA-DRB9 · rs28895136

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, 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 46 Finnish ancestry cases, 18,757 Finnish ancestry controls.

The effect Each copy of the C allele carried 4.13 times the odds of Immunoglobulin A vasculitis (95% confidence interval 3.16-5.38); p = 2 × 10−8.

How common The C allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 6.1 kb from HLA-DRB9.

How common each version is

CT
Korean KRGDB
C 9.1% · T 90.9%
Korean Korea4K
C 8.4% · T 91.6%
Japanese ToMMo
C 5.7% · T 94.3%
Vietnamese
C 7.4% · T 92.6%
World gnomAD
C 12.5% · T 87.5%
World 1000 Genomes
C 12.1% · T 87.9%
World TOPMed
C 11.7% · T 88.3%

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 Immunoglobulin A vasculitis. 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 Immunoglobulin A vasculitis. That is a smaller link than two copies.
T/T No copy of the version the research linked to Immunoglobulin A vasculitis. This is the starting point the study compared everyone against.
Source

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Immunoglobulin A vasculitis (rs28895136). MyGeneLog™. https://www.mygenelog.com/variants/rs28895136

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