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IgA nephropathy

HLA-DRB1 · rs660895

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−19, with 7 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 1,434 Han Chinese ancestry cases, 4,270 Han Chinese ancestry controls; replicated in 2,703 Han Chinese ancestry cases, 3,464 Han Chinese ancestry controls.

The effect Each copy of the G allele carried 1.34 times the odds of IgA nephropathy (95% confidence interval 1.26-1.42); p = 4 × 10−20.

How common The G allele had a frequency of about 24% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 18.6 kb from HLA-DQA1.

How common each version is

AG
Korean KRGDB
A 72.7% · G 27.3%
Korean Korea4K
A 74.0% · G 26.0%
Japanese ToMMo
A 71.2% · G 28.8%
World gnomAD
A 80.5% · G 19.5%
World 1000 Genomes
A 80.2% · G 19.9%
World TOPMed
A 79.8% · G 20.2%

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 IgA nephropathy. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to IgA nephropathy. That is a smaller link than two copies.
G/G Two copies of the version the research linked to IgA nephropathy. 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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IgA nephropathy (rs660895). MyGeneLog™. https://www.mygenelog.com/variants/rs660895

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