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Standard

HLA DR on myeloid Dendritic Cell

near HLA-DQA1 · rs9271367

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−35, with 4 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 2,872 Sardinian (founder/genetic isolate) ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.588 lower (95% confidence interval 0.5-0.68); p = 3 × 10−35.

How common The A allele had a frequency of about 86% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 9 kb from HLA-DQA1.

How common each version is

AG
Korean KRGDB
A 77.2% · G 22.8%
Korean Korea4K
A 75.5% · G 24.5%
Korean Korea1K
A 33.5% · G 66.5%
Japanese ToMMo
A 73.1% · G 26.9%
Vietnamese
A 67.0% · G 33.0%
World gnomAD
A 71.6% · G 28.4%
World 1000 Genomes
A 71.5% · G 28.5%
World TOPMed
A 73.3% · G 26.7%

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 HLA DR on myeloid Dendritic Cell. 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 HLA DR on myeloid Dendritic Cell. That is a smaller link than two copies.
G/G No copy of the version the research linked to HLA DR on myeloid Dendritic Cell. This is the starting point the study compared everyone against.
Source

Quoting this page

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HLA DR on myeloid Dendritic Cell (rs9271367). MyGeneLog™. https://www.mygenelog.com/variants/rs9271367

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