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Synevo

Synevo Laboratories is a healthcare specialist brand since 2002. Every year, Synevo runs approximately 25 million lab tests. Buy a genetic test, receive a DIY saliva sample and get results in 10 working days.

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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

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.

from PLN 1,499.00 Mediclub logo Mediclub logo from PLN 1,420.00
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Analysis of exons 10 and 11 of the RET gene - first stage of diagnostics of medullary thyroid cancer

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

from PLN 572.00 Mediclub logo Mediclub logo from PLN 542.00
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Analysis of exons 10, 11, 15 and 16 of the RET gene - diagnostics of multiple endocrine adenomatosis type 2A and 2B (MEN2A and MEN2B)

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

from PLN 1,000.00 Mediclub logo Mediclub logo from PLN 948.00
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Analysis of exons 16 and 17 of the APP gene - the second stage of diagnostics of hereditary Alzheimer's disease
from PLN 482.00 Mediclub logo Mediclub logo from PLN 456.00
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Analysis of exons 2, 3, 5, 6 and 11 of the NOTCH3 gene - the 2nd stage of CADASIL syndrome diagnostics

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.

from PLN 1,140.00 Mediclub logo Mediclub logo from PLN 1,080.00
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Analysis of exons 2-11 of the NOTCH3 gene - I + II + III for the diagnostics of CADASIL syndrome

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.

from PLN 2,197.00 Mediclub logo Mediclub logo from PLN 2,082.00
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Analysis of exons 5, 8 and 13-16 of the RET gene - second stage of diagnostics of medullary thyroid cancer

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

from PLN 1,300.00 Mediclub logo Mediclub logo from PLN 1,231.00
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Analysis of exons 7, 9, 8 and 11 of the NOTCH3 gene - the 3rd stage of CADASIL syndrome diagnostics

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

from PLN 1,020.00 Mediclub logo Mediclub logo from PLN 967.00
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Analysis of M2 haplotype of ANXA5 gene-diagnosis of recurrent miscarriages

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

from PLN 483.00 Mediclub logo Mediclub logo from PLN 457.00
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Analysis of the (TA)n-repeats region in the UGT1A1 gene promoter (c.-55_-54insTA mutation) - diagnostics of Gilbert's syndrome

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.

PLN 321.00 Mediclub logo Mediclub logo PLN 304.00
Lowest price from 30 days before discounting PLN 203.30

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.