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Standard

Mean platelet volume during third trimester of pregnancy

CD36 · rs12234728

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−16, with 2 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 71,605 Chinese ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.177 lower (95% confidence interval 0.13-0.22); p = 3 × 10−16.

How common The T allele had a frequency of about 7% in the people studied.

Where it sits Chromosome 7, band 7q21.11 — in an intron of CD36.

How common each version is

CT
Korean KRGDB
C 91.0% · T 9.0%
Korean Korea4K
C 90.6% · T 9.4%
Japanese ToMMo
C 87.0% · T 13.0%
Vietnamese
C 93.9% · T 6.1%
World gnomAD
C 99.7% · T 0.3%
World 1000 Genomes
C 98.5% · T 1.5%
World TOPMed
C 99.7% · T 0.3%

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

C/C No copy of the version the research linked to Mean platelet volume during third trimester of pregnancy. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Mean platelet volume during third trimester of pregnancy. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Mean platelet volume during third trimester of pregnancy. 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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Mean platelet volume during third trimester of pregnancy (rs12234728). MyGeneLog™. https://www.mygenelog.com/variants/rs12234728

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