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Standard

Prostate-specific antigen levels

MYO9B · rs10408887

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−9, 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 61,745 African ancestry individuals, 6,967 Asian ancestry individuals, 297,166 European ancestry individuals, 26,644 Hispanic or Latin American individuals.

The effect Each copy of the A allele shifted the measure 0.0118 lower (95% confidence interval 0.008-0.0156); p = 1 × 10−9.

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

How common each version is

AG
Korean KRGDB
A 37.2% · G 62.8%
Korean Korea4K
A 36.2% · G 63.8%
Japanese ToMMo
A 32.4% · G 67.6%
World gnomAD
A 35.6% · G 64.4%
World 1000 Genomes
A 40.8% · G 59.2%
World TOPMed
A 37.7% · G 62.3%

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

A/A Two copies of the version the research linked to Prostate-specific antigen levels. 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 Prostate-specific antigen levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Prostate-specific antigen levels. This is the starting point the study compared everyone against.
Source

Quoting this page

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Prostate-specific antigen levels (rs10408887). MyGeneLog™. https://www.mygenelog.com/variants/rs10408887

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