Biomarkers · Chemical
Hereditary Cancer Single Sites
- Also listed as
- total calcium, serum calcium, Hereditary Cancer Single Site(s), ca
- LOINC codes
- 100761-6, 20990-8, 21636-6, 21739-8, 35474-6, 38530-2, 38536-9, 38550-0, 38906-4, 40693-4, 47969-1, 48004-6, 48018-6, 50397-9, 50398-7, 53037-8, 69047-9, 77202-0, 79419-8, 8266-9, 82939-0
- Tests that measure Hereditary Cancer Single Sites
- Quest Diagnostics 1
Tests
Check the catalog code, specimen, method and preparation for every test that measures Hereditary Cancer Single Sites. Select up to five tests to compare them side by side.
Quest Diagnostics 1 test
Single-analyte tests
Hereditary Cancer Single Site(s) 93945
Blood · Fasting not stated · Turnaround Set up: Tues, Thurs, Sat
Quest Diagnostics catalog pageMethod and collection
- Method
- DNA Bait Capture • Long Range Polymerase Chain Reaction • Next Generation Sequencing • Microarray
- Preparation
- Saliva: Do not eat, drink, smoke or chew gum for 30 minutes before collection. Buccal swab: Please refer to user instructions provided with kit. Ensure the sponge tip does not come into contact with any surface prior to collection. Do not eat, drink, smoke, or chew gum for 30 minutes before collection. Do not touch swab tips or allow contact with any other object.
- Collection
- Do not hold specimen. Forward to laboratory when specimen arrives. Whole blood: Normal phlebotomy procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze. Saliva: 2 mL saliva collected in the Oragene-Dx collection kit up to the "fill to" line (OGD-500/OGD-600, OGD-510/OGD-610). Do not remove the plastic film from the funnel lid. For fibroblasts and skin fibroblasts, call 1-866-GENEINFO (1-866-436-3463) prior to collecting and ordering. For fetal testing 1) Please call 1-866-GENE-INFO (1-866-436-3463) prior to submission 2) Documentation of parental carrier status must be provided 3) It is required that Maternal Cell Contamination Study, STR Analysis be ordered in conjunction with fetal testing. A separate tube of maternal blood (EDTA) is required for this test. Amniocyte or chorionic villus (CVS) culture: Two sterile T25 flasks, 75% confluent, filled with culture medium. Specimen stability is crucial. Store and ship at room temperature immediately. Do not refrigerate or freeze. Forward to laboratory when cells arrive. Amniotic fluid: Normal collection procedure. Specimen stability is crucial. Store and ship room temperature immediately. Do not refrigerate or freeze. Forward to laboratory when sample arrives. Dissected chorionic villus (CVS) biopsy: 10-20 mg dissected chorionic villi collected in sterile tube, filled with sterile culture medium. Specimen stability is crucial. Store and ship at room temperature immediately. Do not refrigerate or freeze. Forward to laboratory when sample arrives.
- Reference notes
- See Laboratory Report
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Quest Diagnostics test catalog
1 test: codes, specimens, methods, preparation and reference intervals.
LOINC 100761-6, 20990-8, 21636-6, 21739-8, 35474-6, 38530-2, 38536-9, 38550-0, 38906-4, 40693-4, 47969-1, 48004-6, 48018-6, 50397-9, 50398-7, 53037-8, 69047-9, 77202-0, 79419-8, 8266-9, 82939-0
Regenstrief Institute codes that identify the same result across labs.
Search ClinicalTrials.gov for Hereditary Cancer Single Sites
Registered studies that measure Hereditary Cancer Single Sites, on the U.S. National Library of Medicine registry.
Verify these ranges and sources
We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.
Interpret your own results with a licensed clinician, or track your lab history and health goals in Aumnivida.
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