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Serum parathyroid hormone levels

RTDR1 · rs4443100

What the study found

Who was studied up to 22,653 European ancestry individuals.; replicated in 6,502 European ancestry individuals..

The effect Each copy of the G allele shifted the measure 0.02 higher (95% confidence interval 0.014-0.026); p = 4 × 10−11.

How common The G allele had a frequency of about 32% in the people studied.

Where it sits Chromosome 22, band 22q11.22 — between genes, 28.7 kb from RSPH14.

What each result means

C/C No copy of the version the research linked to Serum parathyroid hormone levels. This is the starting point the study compared everyone against.
C/G One copy of the version the research linked to Serum parathyroid hormone levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Serum parathyroid hormone levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs4443100

What is rs4443100?

rs4443100 is a single position in the genome, in or near the RTDR1 gene. Published research associates it with serum parathyroid hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4443100 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 rs4443100 come from?

GWAS Catalog, Journal of the American Society of Nephrology : JASN 2017, PMID:27927781. 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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Serum parathyroid hormone levels (rs4443100). MyGeneLog™. https://www.mygenelog.com/variants/rs4443100

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