- Home
- Health Tests
- Allergy
- Anaemia
- Andrology
- Autoimmune
- Biochemistry
- Blood Clotting
- Blood Group
- Bone Health
- Bowel Health
- Cancer Related
- Cardiac Health
- Coagulation
- Diabetes
- Fertility
- Genetics
- Haematology
- Health Checks
- Hormones
- Immunity
- Immunology
- Infections
- Inflamations
- Liver Health
- Men's Health
- Microbiology
- Molecular Biology
- Occupational Health
- Pathology
- Pregnancy
- Screen for Drug of Abuse
- Sexual Health
- Thyroid Health
- Vitamins
- Vitamins and Minerals
- Women's Health
- Genetic Tests
- MBMC
- MBMSK
- Aesthetic medicine
- Allergology
- Anatomical Pathology
- Andrology
- Bone Skin And Immune Diseases
- Cardiology
- Cardiovascular
- Custom Panel
- Cytohistology
- Dentistry
- Dermatology
- Endocrinology
- Forensic
- Gastroenterology
- Geriatrics
- Gynecology
- Hematology
- Hepatology
- Immunology
- Infectiology
- Infectivology
- Maxillofacial surgery
- Metabolic diseases
- Miscellaneous
- Neonatology
- Nephrology
- Neurology
- Nutrigenetics
- Nutrition
- Oncology
- Ophthalmology
- Orthopedics
- Otolaryngology
- Pediatrics
- Pharmacogenetics
- Pneumology
- Prenatal
- Reproduction
- Rheumatology
- Senology
- Sports medicine
- Urology
- PrenatalSAFE® NIPT
- Cancer Screening
- Kits & Supplies
- Services
- About Us
- 0
- £0.000
- Sign in
congenital Deafness (panel), Autosomal dominant non-syndromic sensorineural deafness type DFNA, Autosomal recessive type DFNB
Call to order - 01707 707 560.
Online order will be available soon.
Description
External Information
Click here for more information about the congenital Deafness (panel), Autosomal dominant non-syndromic sensorineural deafness type DFNA, Autosomal recessive type DFNB genetic test.Additional information
Samples | EDTA, LA, VC |
---|---|
Method of testing | NGS |
Turnaround Time (TAT) | 30-40 days |
Number of Genes | 101 |
Genes / Chromosomes / SNPs | ACTG1, AIFM1, ATP6V1B1, BSND, CCDC50, CDH23, CEACAM16, CIB2, CISD2, CLDN14, CLRN1, COCH, COL11A1, COL11A2, COL2A1, COL9A1, COL9A2, CRYM, DCDC2, DFNA5, DFNB31, DFNB59, DIABLO, DIAPH1, DIAPH3, EDN3, EDNRB, ESPN, ESRRB, EYA1, EYA4, FOXI1, GIPC3, GJB2, GJB3, GJB6, GPR98, GRHL2, GRXCR1, HARS, HGF, HOMER2, ILDR1, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, KITLG, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MITF, MSRB3, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NARS2, OPA1, OTOA, OTOF, PAX3, PCDH15, PDZD7, POLR1C, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, SERPINB6, SIX1, SIX5, SLC17A8, SLC26A4, SLC26A5, SMPX, SNAI2, SOX10, STRC, TBC1D24, TCOF1, TECTA, TJP2, TMC1, TMIE, TMPRSS3, TNC, TPRN, TRIOBP, USH1C, USH1G, USH2A, WFS1 |
External Information | Click here for more information about the congenital Deafness (panel), Autosomal dominant non-syndromic sensorineural deafness type DFNA, Autosomal recessive type DFNB genetic test. |