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Pyogenic granuloma (PheCode 686.4)

LINC01698 · rs368835767

Where this position leads

Condition: Pyogenic Granuloma

rs368835767 Condition: Pyogenic Granuloma Pyogenic Granuloma Condition rs368835767 rs368835767 LINC01698

What the study found

Who was studied 275 African American or Afro-Caribbean cases, 121,138 African American or Afro-Caribbean controls, 790 European ancestry cases, 448,371 European ancestry controls.

The effect Each copy of the C allele shifted the measure 4.13 lower (95% confidence interval 4.12-4.14); p = 2 × 10−13.

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

Where it sits Chromosome 1, band 1q32.2 — in an intron of LINC01698.

What each result means

C/C Two copies of the version the research linked to Pyogenic granuloma (PheCode 686.4). 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 Pyogenic granuloma (PheCode 686.4). That is a smaller link than two copies.
T/T No copy of the version the research linked to Pyogenic granuloma (PheCode 686.4). This is the starting point the study compared everyone against.
Source

Questions about rs368835767

What is rs368835767?

rs368835767 is a single position in the genome, in or near the LINC01698 gene. Published research associates it with pyogenic granuloma (phecode 686.4). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs368835767 linked to?

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

Does having rs368835767 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 rs368835767 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

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Pyogenic granuloma (PheCode 686.4) (rs368835767). MyGeneLog™. https://www.mygenelog.com/variants/rs368835767

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