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Who was studied 28,106 European, African, Admixed American, East Asian, South Asian or unknown ancestry individuals (MTAG effective sample size boosted by left ventricular trait samples).
The effect
Each copy of the G allele shifted the measure 0.184 higher (95% confidence interval 0.14-0.23); p = 2 × 10−15.
How common The G allele had a frequency of about 74% in the people studied.
Where it sits Chromosome 12, band 12q24.21 — between genes, 156.1 kb from TBX3-AS1.
What each result means
A/ANo copy of the version the research linked to Hypertrophic cardiomyopathy (MTAG). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Hypertrophic cardiomyopathy (MTAG). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Hypertrophic cardiomyopathy (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2025 · PMID 39966646 · open access
Questions about rs7487962
What is rs7487962?
rs7487962 is a single position in the genome, in or near the near TBX3-AS1 gene. Published research associates it with hypertrophic cardiomyopathy (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7487962 linked to?
On MyGeneLog this position is linked to Hypertrophic Cardiomyopathy. The research behind each link, and its sources, are set out on that condition page.
Does having rs7487962 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 rs7487962 come from?
GWAS Catalog, Nature genetics 2025, PMID:39966646. 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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