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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
Strength of the evidence
1 / 4
Its strongest genetic-study result is p = 10−11, 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 164,339 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0286 higher (95% confidence interval 0.021-0.037); p = 5 × 10−12.
How common The T allele had a frequency of about 27% in the people studied.
Where it sits Chromosome 22, band 22q11.21 — in an intron of TANGO2.
How common each version is
CT
KoreanKRGDB
C 91.4% · T 8.6%
KoreanKorea4K
C 91.6% · T 8.3%
Japanese ToMMo
C 87.5% · T 12.5%
World gnomAD
C 77.9% · T 22.1%
World 1000 Genomes
C 80.7% · T 19.3%
World TOPMed
C 79.1% · T 20.9%
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/CNo copy of the version the research linked to Plateletcrit. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Plateletcrit. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Plateletcrit. That is the strongest link of the three results. A link in a study is not a diagnosis.
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Quoting this page
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