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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 288,127 East Asian ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0371 higher (95% confidence interval 0.031-0.043); p = 2 × 10−30.
How common The A allele had a frequency of about 33% in the people studied.
Where it sits Chromosome 2, band 2q31.1 — in an intron of ABCB11.
What each result means
A/ATwo copies of the version the research linked to Gamma glutamyl transferase 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 Gamma glutamyl transferase levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Gamma glutamyl transferase levels. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 36333282 · open access
Questions about rs72623176
What is rs72623176?
rs72623176 is a single position in the genome, in or near the ABCB11 gene. Published research associates it with gamma glutamyl transferase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs72623176 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 rs72623176 come from?
GWAS Catalog, Nature communications 2022, PMID:36333282. 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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