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Standard

Blond vs. brown/black hair color

EXOC2 · rs6918152

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−59, 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 39,397 British ancestry blond hair individuals, 283,920 British ancestry brown or black hair individuals.

The effect The reported allele is A; the catalogue records no effect size ; p = 2 × 10−59.

How common The A allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 6, band 6p25.3 — in an intron of EXOC2.

How common each version is

AG
Korean KRGDB
A 53.2% · G 46.8%
Korean Korea4K
A 51.5% · G 48.5%
Korean Korea1K
A 52.8% · G 47.2%
Japanese ToMMo
A 41.6% · G 58.4%
Vietnamese
A 59.4% · G 40.6%
World gnomAD
A 52.0% · G 48.0%
World 1000 Genomes
A 53.5% · G 46.5%
World TOPMed
A 53.8% · G 46.2%

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 Blond vs. brown/black hair color. 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 Blond vs. brown/black hair color. That is a smaller link than two copies.
G/G No copy of the version the research linked to Blond vs. brown/black hair color. This is the starting point the study compared everyone against.
Source

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Blond vs. brown/black hair color (rs6918152). MyGeneLog™. https://www.mygenelog.com/variants/rs6918152

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