mdd-dna-kit-min

Inherited Cancer Panel

$1,250.00

Gain peace of mind with our Inherited Cancer Panel, the definitive screening test for those worried about hereditary cancers, such as breast, ovarian, prostate, colorectal (bowel), and skin cancers. This comprehensive screening analyses 130 different genes associated with various hereditary cancers, testing for the most common mutations.

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Description

Mobile Drug & DNA has streamlined the DNA test process:

  1. Order your test online.
  2. Complete payment.
  3. As part of our process, we require that you consult with a genetic counsellor both before and after undergoing the test. Mobile Drug & DNA will facilitate this by requesting a referral form to be completed by your GP, genetic counselor, or specialist.
  4. When you order the Inherited Cancer Panel, we will provide you with the necessary referral forms for your genetic counsellor or doctor to fill out. Subsequently, we will arrange for your sample collection kit to be sent directly to one of our affiliated pathology centers and schedule your appointment for sample collection.
  5. Following the analysis, your results will be sent to your genetic counsellor or doctor. They will then thoroughly discuss the results with you, ensuring you receive the best and most accurate information tailored to your individual test.

About The Test

Cancer touches the lives of everyone in some way. Whether through personal experience or knowing someone affected by it, we’ve all felt its impact. While some cancers arise due to a combination of chance and environmental factors, up to 10% are associated with inherited gene mutations passed down from relatives.

These hereditary cancers, caused by genetic mutations, often manifest earlier and can be more aggressive than non-hereditary forms. Our DNA, comprising nucleotides carrying instructions for protein synthesis, can undergo mutations that alter protein function, leading to the emergence of new genetic traits, disorders, or diseases.

Samples

This straightforward test involves a blood draw, from which your DNA is extracted and analysed using Next Generation Sequencing technology. The blood draw must be conducted by a qualified sample collector, with associated additional costs.

It’s essential to highlight that undergoing this test also necessitates attending a genetic counselling session with a qualified professional. Your counsellor will receive your results and discuss them with you at a mutually convenient time. Additionally, the genetic counselling session ensures that you receive comprehensive guidance and support throughout the testing process.

Panels

IP, AKT1, ALK, ANTXR1, APC, ASCC1, ATM, ATR, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, BUB1, BUB1B, CACNA1D, CBL, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, CTHRC1, CYLD, DDB2, DICER, EGFR, ELAC2, EPCAM, ERCC2, ERCC3, ERCC4, ERCC5, EXT1, EXT2, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FH, FLCN, GPC3, HNF1A, HNF1B, HOXB13, KDR, KIT, KLLN, LIG4, MAX, MEN1, MET, MITF, MLH1, MLH3, MRE11A, MSH2, MSH6, MSR1, MTAP, MUTYH, MYH8, NBN, NCOA4, NF1, NF2, NTRK1, PALB2, PALLD, PDGFRB, PHOX2B, PIK3CA, PMS2, POLD1, POLE, POLH, PPM1D, PRF1, PRKAR1A, PRSS1, PTCH1, PTCH2, PTEN, PTPN11, RAD50, RAD51C, RAD51D, RB1, RECQL4, RET, RHBDF2, RNASEL, RNF168, RSPO1, RUNX1, SBDS, SDHA, SDHAF2, SDHB, SDHC, SDHD, SETBP1, SH2D1A, SLX4, SMAD4, SMARCB1, SMARCE1, SPINK1, SPRED1, STK11, SUFU, TERT, TGFBR1, TMEM127, TP53, TSC1, TSC2, VHL, WAS, WRN, WT1, XPA, XPC, XRCC2.

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