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near CBFA2T3 · rs530238572
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
Its strongest genetic-study result is p = 10−94, with 2 associations in the GWAS Catalog.
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 20,692 European ancestry cases, 434,472 European ancestry controls.
The effect Each copy of the C allele shifted the measure 2.83 higher (95% confidence interval 2.56-3.1); p = 4 × 10−95.
How common The C allele had a frequency of about 0% in the people studied.
Where it sits Chromosome 16, band 16q24.3 — between genes, 11.4 kb from CBFA2T3.
How common each version is
CT
C 0.1% · T 99.9%
C 0.1% · T 99.9%
C 0.1% · T 99.9%
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. No Korean figure for this position yet.
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Hair colour (natural, before greying): Red (UKB data field 1747_2) (rs530238572). MyGeneLog™. https://www.mygenelog.com/variants/rs530238572