Cardiology Panel NGS Genetic Test
At DNA Labs UAE, we offer the Cardiology Panel NGS Genetic Test at a cost of AED 4400.0. This test analyzes a patient’s DNA for mutations and variations in genes associated with cardiovascular disease.
Test Details
The Cardiology Panel NGS Genetic DNA Test is a genetic test that uses next-generation sequencing (NGS) technology to analyze multiple genes at once. By identifying genetic variants, this test can help assess the risk of developing conditions such as coronary artery disease, arrhythmias, and cardiomyopathies.
Components
- Test Name: Cardiology Panel NGS Genetic DNA Test
- Price: AED 4400.0
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Cardiovascular Pneumology Disorders
- Doctor: Cardiologist
- Test Department: Genetics
Pre-Test Information
Before undergoing the Cardiology Panel NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with various genetic conditions associated with cardiovascular disease.
Benefits
The results from the Cardiology Panel NGS Genetic Test can provide valuable information for medical management decisions and guide preventative measures. By identifying genetic variants, healthcare professionals can develop personalized treatment plans and interventions to reduce the risk of cardiovascular disease.
Conclusion
The Cardiology Panel NGS Genetic Test offered by DNA Labs UAE is a comprehensive genetic test that can assess the risk of developing cardiovascular disease. With its advanced NGS technology and thorough analysis of multiple genes, this test provides valuable insights for medical management and prevention strategies. Contact DNA Labs UAE today to schedule your Cardiology Panel NGS Genetic Test.
Test Name | Cardiology Panel NGS Genetic DNA Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Cardiovascular Pneumology Disorders |
Doctor | Cardiologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for Cardiology Panel NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCC9, ACTA2, ACTC1, ACTN2, ACVR2B, ACVRL1, AKAP9, ANK2, ANKRD1, ARHGAP31, ATM, B3GAT3, BAG3, BCOR, BMPR2, BRAF, CACNA1C, CACNB2, CALM1, CALM2, CASQ2, CAV3, CAVIN4, CBL, CDH2, CFAP53, CFC1, CHD7, CITED2, CLDN16, CLDN19, CNNM2, COL1A1, COL1A2, COL3A1, COL4A1, COL4A2, COL5A1, COL5A2, CREBBP, CRELD1, CRYAB, CSRP3, CTNNA3, DES, DMD, DNAJC19, DOLK, DSC2, DSG2, DSP, DTNA, EFEMP2, EGF, EHMT1, ELN, EMD, ENG, EP300, EVC, EVC2, EYA4, FBN1, FBN2, FHL1, FKTN, FLNA, FLNC, FOXC1, FOXF1, FOXH1, FXYD2, GAA, GATA4, GATA5, GATA6, GDF1, GDF2, GJA1, GJA5, GLA, GPC3, GPD1L, HCCS, HCN4, HFE, HRAS, HTRA1, ILK, JAG1, JPH2, JUP, KCNA1, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNK3, KCNQ1, KDM6A, KMT2D, KRAS, LAMA4, LAMP2, LDB3, LMNA, LZTR1, MAP2K2, MED12, MED13L, MEIS2, MFAP5, MIB1, MMP21, MMP3, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYLK2, MYO6, MYOZ2, MYPN, NEBL, NEXN, NF1, NIPBL, NKX2-5, NKX2-6, NODAL, NOTCH1, NOTCH2, NOTCH3, NPPA, NR2F2, NRAS, NSD1, PDLIM3, PKD1L1, PKD2, PKP2, PLN, PRDM16, PRKAG2, PRKG1, PSEN1, PSEN2, PTPN11, RAF1, RASA1, RBM10, RBM20, RIT1, RYR2, SALL1, SALL4, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCO2, SDHA, SEMA3A, SGCD, SHOC2, SKI, SLC12A3, SLC22A5, SLC25A4, SLC2A10, SLMAP, SMAD3, SMAD4, SMAD6, SMC3, SNTA1, SOS1, SOS2, SOX2, STRA6, SYNE1, SYNE2, TAB2, TAZ, TBX1, TBX20, TBX5, TCAP, TFAP2B, TGFB2, TGFB3, TGFBR1, TGFBR2, TLL1, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TREX1, TRIM63, TRPM4, TRPM6, TTN, TTR, VCL, ZEB2, ZFPM2, ZIC3 |
Test Details | The Cardiology Panel NGS Genetic DNA Test is a genetic test that analyzes a patient’s DNA for mutations and variations in genes associated with cardiovascular disease. This test is performed using next-generation sequencing (NGS) technology, which allows for the analysis of multiple genes at once. The test can identify genetic variants that increase the risk of developing conditions such as coronary artery disease, arrhythmias, and cardiomyopathies. Results from this test can help inform medical management decisions and guide preventative measures for patients with a genetic predisposition to cardiovascular disease. |