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Accession: PRJNA475606 ID: 475606

Homo sapiens (human)

CDKN2A Germline Rare Coding Variants and Risk of Pancreatic Cancer in Minority Populations

See Genome Information for Homo sapiens
The study reports rare germline variants in the CDKN2A gene and its associated risk of pancreatic cancer.
AccessionPRJNA475606
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Grants
  • "Genetic Epidemiology of Young-Onset Pancreatic Cancer" (Grant ID K07 CA116303, National Cancer Institute)
  • "Mayo Clinic SPORE in Pancreatic Cancer" (Grant ID P50 CA102701, National Cancer Institute)
  • "Pancreatic Cancer Genetic Epidemiology Consortium (PACGENE)" (Grant ID R01 CA097075, National Cancer Institute)
  • "Mayo Cancer Genetic Epidemiology Training Program" (Grant ID R25 CA092049, National Cancer Institute)
SubmissionRegistration date: 11-Jun-2018
Mayo Clinic
RelevanceMedical
Project Data:
No public data is linked to this project. Any recently released data that cites this project will be linked to it within a few days.

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