Medical Genetics Test Details
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Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 2 tests available.
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Diagnostic Testing | Familial Mutation/Variant Analysis | Mutation Testing General Population | Prenatal Diagnosis | Presymptomatic Testing | |
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Sequence Analysis |
![]() Test Code: 5395 |
![]() Test Code: 5396 This test can only be performed if there is a previously identified familial mutation. |
![]() Test Code: 5397 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363. |
HNRNPA2B1 Sequence Analysis (Prenatal Diagnosis) |
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Test Information: | Prenatal Diagnosis - Known Familial Mutation(s) | |
Test Details | ||
Test Code: | 5397 | |
Test Includes: |
Sequencing of the region(s) containing the familial alteration(s) | |
Special Notes: | We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363. | |
Technical Information | ||
Methodology: | Targeted Capture followed by Massively Parallel Sequencing | |
Gene Name: | HNRNPA2B1 | |
Protein Name: | Heterogeneous Nuclear Ribonucleoprotein A2/B1 | |
Test Type: | Sequence Analysis |
Sample & Shipping Information | ||
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Test Requisition: | Prenatal Comprehensive | |
Specimen Type: | Specimen Information | |
Requirements: | Requirements Information | |
Shipping Conditions: | Ship at ambient temperature in an insulated container by overnight courier. |
Turn Around Time: | 21 days | |
Billing Information | ||
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List Price: | *For Insurance or Institutional Prices, please call. | |
CPT Codes: | 81479x1, 81265x1, 81266x1 |