Analysis of activating somatic mutations in codons 12, 13, 59, 61, 117 and 146 of the NRAS gene with a sensitivity of 1% in cancer cells
The test involves analyzing DNA from tumor cellsórecords due to the listed mutations in the KRAS gene, often found in cases of colorectal cancer, and helps predict the course of the disease and response to drugs.
Analysis of exons 10 and 11 of the RET gene - first stage of diagnostics of medullary thyroid cancer
Familial medullary thyroid cancer is a rare cancer predisposition syndrome, accounting for about 5-10% of thyroid cancers
Analysis of exons 10, 11, 15 and 16 of the RET gene - diagnostics of multiple endocrine adenomatosis type 2A and 2B (MEN2A and MEN2B)
Multiple endocrine neoplasia type 2 is a rare cancer predisposition syndrome, with an estimated incidence of 1:35,000
Analysis of exons 2, 3, 5, 6 and 11 of the NOTCH3 gene - the 2nd stage of CADASIL syndrome diagnostics
The study analyzes exons 2, 3, 5, 6, and 11 of a gene associated with an inherited vascular and cerebrovascular disease called CADASIL syndrome, as a second step in diagnosing the disease.
Analysis of exons 2-11 of the NOTCH3 gene - I + II + III for the diagnostics of CADASIL syndrome
Genetic testing includes analysis of exonsó2-11 of the NOTCH3 gene as part of the three-stepódiagnosis of CADASIL syndrome, a disease of the small arterial vessels of the móheart.
Analysis of exons 5, 8 and 13-16 of the RET gene - second stage of diagnostics of medullary thyroid cancer
The second step in the genetic diagnosis of medullary thyroid cancer is genetic testing, which involves detecting certain changes in the genetic material (DNA), namely mutations in the RET gene, whichóre likely to affect the development of the genetic disease, a hereditary form of thyroid cancer
Analysis of exons 7, 9, 8 and 11 of the NOTCH3 gene - the 3rd stage of CADASIL syndrome diagnostics
The study analyzes exonsó7-10 of the NOTCH3 gene as the third step in the diagnosis of a hereditary vascularófatal disease called CADASIL syndrome
Analysis of M2 haplotype of ANXA5 gene-diagnosis of recurrent miscarriages
Helps to identify the causes of recurrent miscarriages and also allow to determine the risk of recurrent miscarriages associated with this gene
Analysis of the (TA)n-repeats region in the UGT1A1 gene promoter (c.-55_-54insTA mutation) - diagnostics of Gilbert's syndrome
Gilbert's syndrome is a common genetic disorder and belongs to the fluke of congenital jaundice with a mild course.
Synevo
As specialists in the health industry, Synevo Laboratories has been in existence since 2002. It performs around 25 million laboratory tests every year. You can buy a genetic test today, get a mail-order saliva sample kit and enjoy the result within 10 working days.
Synevo tests are carried out in Poland, Germany, Turkey, Romania, Ukraine, Georgia, Moldova, Belarus, Russia, Bulgaria and Serbia.