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Standard

Reticulocyte fraction of red cells

MYO9B · rs7246865

Strength of the evidence

2 / 4

Its strongest genetic-study result is p = 10−27, with 19 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 170,690 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0243 higher (95% confidence interval 0.016-0.032); p = 4 × 10−9.

How common The A allele had a frequency of about 26% in the people studied.

Where it sits Chromosome 19, band 19p13.11 — in an intron of MYO9B.

How common each version is

AG
Korean KRGDB
A 37.3% · G 62.7%
Korean Korea4K
A 36.5% · G 63.5%
Japanese ToMMo
A 32.4% · G 67.6%
Vietnamese
A 33.0% · G 67.0%
World gnomAD
A 35.7% · G 64.3%
World 1000 Genomes
A 41.6% · G 58.4%
World TOPMed
A 37.9% · G 62.1%

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 Reticulocyte fraction of red cells. 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 Reticulocyte fraction of red cells. That is a smaller link than two copies.
G/G No copy of the version the research linked to Reticulocyte fraction of red cells. This is the starting point the study compared everyone against.
Source

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Reticulocyte fraction of red cells (rs7246865). MyGeneLog™. https://www.mygenelog.com/variants/rs7246865

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