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Heart rate variability (root mean square of successive differences)

near Y_RNA · rs1906263

What the study found

Who was studied 46,075 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.427 lower (95% confidence interval 0.42-0.43); p = 9 × 10−11.

Where it sits Chromosome 12, band 12q12 — between genes, 14.9 kb from Y_RNA.

What each result means

C/C Two copies of the version the research linked to Heart rate variability (root mean square of successive differences). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Heart rate variability (root mean square of successive differences). That is a smaller link than two copies.
T/T No copy of the version the research linked to Heart rate variability (root mean square of successive differences). This is the starting point the study compared everyone against.
Source

Questions about rs1906263

What is rs1906263?

rs1906263 is a single position in the genome, in or near the near Y_RNA gene. Published research associates it with heart rate variability (root mean square of successive differences). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1906263 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 rs1906263 come from?

GWAS Catalog, Communications biology 2023, PMID:37803156. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Heart rate variability (root mean square of successive differences) (rs1906263). MyGeneLog™. https://www.mygenelog.com/variants/rs1906263

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