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Standard

Immunoglobulin A vasculitis

near MTCO3P1 · rs17427445

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 A allele carried 4.23 times the odds of Immunoglobulin A vasculitis (95% confidence interval 3.24-5.52); p = 1 × 10−8.

How common The A allele had a frequency of about 20% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 10.1 kb from MTCO3P1.

How common each version is

AG
Korean KRGDB
A 8.8% · G 91.2%
Korean Korea4K
A 8.4% · G 91.6%
Japanese ToMMo
A 5.6% · G 94.4%
World gnomAD
A 13.2% · G 86.9%
World 1000 Genomes
A 12.0% · G 88.0%
World TOPMed
A 12.6% · G 87.4%

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 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.
A/G One copy of the version the research linked to Immunoglobulin A vasculitis. That is a smaller link than two copies.
G/G 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 (rs17427445). MyGeneLog™. https://www.mygenelog.com/variants/rs17427445

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