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Hearing difficulty

PDCD6-AHRR · rs537688122

What the study found

Who was studied 45,502 European ancestry cases, 96,601 European ancestry controls.

The effect Each copy of the G allele shifted the measure 1.35 higher (95% confidence interval 1.08-1.62); p = 1 × 10−21.

How common The G allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 5, band 5p15.33 — a synonymous change in PDCD6-AHRR.

What each result means

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

Questions about rs537688122

What is rs537688122?

rs537688122 is a single position in the genome, in or near the PDCD6-AHRR gene. Published research associates it with hearing difficulty. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs537688122 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 rs537688122 come from?

GWAS Catalog, European journal of human genetics : EJHG 2023, PMID:36788145. 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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Hearing difficulty (rs537688122). MyGeneLog™. https://www.mygenelog.com/variants/rs537688122

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