Sensitive

Neuroendocrine tumors (PheCode 209)

near RNU6-1120P · rs192006671

Where this position leads

Condition: Neuroendocrine Tumors

rs192006671 Condition: Neuroendocrine Tumors Neuroendocrine Tumors Condition rs192006671 rs192006671 near RNU6-11…

What the study found

Who was studied 211 African American or Afro-Caribbean cases, 121,601 African American or Afro-Caribbean controls, 540 European ancestry cases, 450,490 European ancestry controls.

The effect Each copy of the T allele shifted the measure 3.62 lower (95% confidence interval 3.6-3.64); p = 3 × 10−11.

How common The T allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 3, band 3q26.32 — between genes, 29.2 kb from RNU6-1120P.

What each result means

C/C No copy of the version the research linked to Neuroendocrine tumors (PheCode 209). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Neuroendocrine tumors (PheCode 209). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Neuroendocrine tumors (PheCode 209). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs192006671

What is rs192006671?

rs192006671 is a single position in the genome, in or near the near RNU6-1120P gene. Published research associates it with neuroendocrine tumors (phecode 209). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs192006671 linked to?

On MyGeneLog this position is linked to Neuroendocrine Tumors. The research behind each link, and its sources, are set out on that condition page.

Does having rs192006671 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 rs192006671 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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Neuroendocrine tumors (PheCode 209) (rs192006671). MyGeneLog™. https://www.mygenelog.com/variants/rs192006671

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