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Intraductal papillary mucinous neoplasm

near NUP35P2 · rs117620617

What the study found

Who was studied 338 European ancestry individuals.

The effect Each copy of the T allele carried 13.15 times the odds of Intraductal papillary mucinous neoplasm (95% confidence interval 5.69-30.39); p = 2 × 10−9.

Where it sits Chromosome 7, band 7q21.11 — between genes, 29.4 kb from NUP35P2.

What each result means

C/C No copy of the version the research linked to Intraductal papillary mucinous neoplasm. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Intraductal papillary mucinous neoplasm. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Intraductal papillary mucinous neoplasm. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs117620617

What is rs117620617?

rs117620617 is a single position in the genome, in or near the near NUP35P2 gene. Published research associates it with intraductal papillary mucinous neoplasm. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs117620617 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 rs117620617 come from?

GWAS Catalog, Cancer 2025, PMID:39639588. 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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Intraductal papillary mucinous neoplasm (rs117620617). MyGeneLog™. https://www.mygenelog.com/variants/rs117620617

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