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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 96,562 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.041 higher (95% confidence interval 0.031-0.051); p = 3 × 10−15.
How common The T allele had a frequency of about 32% in the people studied.
Where it sits Chromosome 8, band 8p23.1 — inside PPP1R3B-DT.
What each result means
C/CNo copy of the version the research linked to Spatial QRS-T angle. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Spatial QRS-T angle. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Spatial QRS-T angle. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2023 · PMID 36918541 · open access
Questions about rs330944
What is rs330944?
rs330944 is a single position in the genome, in or near the PPP1R3B-DT gene. Published research associates it with spatial qrs-t angle. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs330944 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 rs330944 come from?
GWAS Catalog, Nature communications 2023, PMID:36918541. 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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