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P16 (CDKN2A) Deletion P16, 9p21.3, Red D9Z3, 9q12, Greene: RUMP 030 / RUMP 031 / RUMP 032 / RUMP 033Multiprobe ALL Panel v2 (RUN)Research Use Only PROFESSIONAL USE ONLY Further information available
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p16 cdkn2 is a tumor suppressor protein that is encoded by the CDKN2A gene. It plays a critical role in regulating the cell cycle and preventing uncontrolled cell division.
Filing for p16 cdkn2 is typically required for individuals or entities that need to report genetic testing results related to the presence of the CDKN2A gene, often in the context of hereditary cancer risk assessments.
To fill out the p16 cdkn2 form, one must gather all relevant medical and family history, complete personal identification sections, and provide specific details regarding genetic testing results if applicable.
The purpose of p16 cdkn2 is to document and report on genetic information that may indicate an increased risk of certain cancers, especially melanoma, and to guide further medical surveillance and preventive measures.
Information that must be reported on p16 cdkn2 includes personal health data, family history of cancer, genetic test results for the CDKN2A gene, and any preventive measures that may be recommended.
The penalty for late filing of p16 cdkn2 may include fines, additional reporting requirements, and potential negative impacts on medical care or insurance coverage, depending on relevant regulations.
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