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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.
What the study found
Who was studied 6,257 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.26 higher (95% confidence interval 0.18-0.34); p = 6 × 10−11.
How common The A allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 6, band 6p21.33 — between genes, 1.4 kb from HCP5.
What each result means
A/ATwo copies of the version the research linked to Flavin adenine dinucleotide (FAD) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Flavin adenine dinucleotide (FAD) levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Flavin adenine dinucleotide (FAD) levels. This is the starting point the study compared everyone against.
rs62395307 is a single position in the genome, in or near the near HCP5 gene. Published research associates it with flavin adenine dinucleotide (fad) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs62395307 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs62395307 come from?
GWAS Catalog, Nature genetics 2023, PMID:36635386. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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