Renal Cancer Panel Build info
Synonyms |
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Short Name |
RENAL CANCER PANEL |
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Procedure Master Number |
LAB155109 |
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Procedure ID |
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Clinical Info |
This test is appropriate for patients to verify the genetic basis of cancer in families indicative or suggestive of a predisposition to renal cancer. VHL, MET, FLCN, FH, TSC1 and TSC2 are the genes that are the most often associated with classic forms of hereditary renal cancer, there are several other genes that cause an increased risk of renal cancer. For example, if the family history consists of multiple types of cancer, such as renal cancer in addition to pancreatic cancer, this may be associated with a cancer syndrome such as VHL or Lynch syndrome. Results may help in determining treatment and management, as well as identification of at-risk family members. |
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Specimen Sources |
Blood, Arterial Blood, Capillary Blood, Central Line Blood, Venous | ||||||||
Specimen Types |
Blood | ||||||||
Container |
Lavender Top Tube or Buccal (Oral Cheek Swab) |
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Collection Instructions |
Container/Tube: Lavender top tube |
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Transport Instructions |
Room Temperature |
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Specimen Stability |
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Methodology |
Genotyping by Next Generation Sequencing |
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Days Performed |
TAT: 21-29 Days |
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Performing Laboratory |
GeneDx |
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CPT |
81435 |
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PDM |
1659884 | ||||||||
Only Orderable at Locations: |
Orderable Everywhere | ||||||||
Results |
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Forms |
