Sensitive

Tumor necrosis factor receptor superfamily member 6 levels

near HLA-DQA1 · rs34967069

What the study found

Who was studied 21,758 European ancestry individuals; replicated in 9,173 individuals.

The effect Each copy of the T allele shifted the measure 0.138 higher; p = 3 × 10−20.

How common The T allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 4.7 kb from HLA-DQA1.

What each result means

C/C No copy of the version the research linked to Tumor necrosis factor receptor superfamily member 6 levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Tumor necrosis factor receptor superfamily member 6 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Tumor necrosis factor receptor superfamily member 6 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs34967069

What is rs34967069?

rs34967069 is a single position in the genome, in or near the near HLA-DQA1 gene. Published research associates it with tumor necrosis factor receptor superfamily member 6 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs34967069 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 rs34967069 come from?

GWAS Catalog, Nature metabolism 2020, PMID:33067605. 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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Tumor necrosis factor receptor superfamily member 6 levels (rs34967069). MyGeneLog™. https://www.mygenelog.com/variants/rs34967069

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