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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 181,862 European ancestry elderly individuals.
The effect
Each copy of the C allele shifted the measure 0.0564 higher (95% confidence interval 0.04-0.073); p = 2 × 10−11.
How common The C allele had a frequency of about 79% in the people studied.
Where it sits Chromosome 13, band 13q22.3 — in an intron of EDNRB-AS1.
What each result means
C/CTwo copies of the version the research linked to Appendicular lean mass. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Appendicular lean mass. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Appendicular lean mass. This is the starting point the study compared everyone against.
American journal of human genetics · 2019 · PMID 31761296
Questions about rs1146933
What is rs1146933?
rs1146933 is a single position in the genome, in or near the EDNRB-AS1 gene. Published research associates it with appendicular lean mass. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1146933 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 rs1146933 come from?
GWAS Catalog, American journal of human genetics 2019, PMID:31761296. 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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Quoting this page
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Appendicular lean mass (rs1146933). MyGeneLog™. https://www.mygenelog.com/variants/rs1146933