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₾1,840.50
Samples will be sent on Friday afternoon! For this, the sample must be sent to the central laboratory by Friday 12:00.
For interpreting research resultsLaboratory""Synevo"We offer MEDICOVER GeneticsGeneticist's freeConsultation
The Thrombophilia and Neonatal Alloimmune Thrombocytopenia (NAIT) panel identifies genetic variations that increase the risk of conditions such as:
(Neonatal alloimmune thrombocytopenia (NAIT) is a rare but serious condition in newborns caused by the mother's immune system attacking the fetus' platelets during pregnancy.)
The panel ensures the identification of individuals at risk before life-threatening conditions develop, allowing for management of the condition and reduction of complications.
Rodinia – Thrombophilia and NAIT Panel (standalone panel) can be used both individually and as an additional test in male and female infertility panel studies.
How many genes are being studied?
The panel will examine 22 genetic variants in 17 genes
Study sample:Cheek swab
genes
NM_000130.4(F5):c.1601G>A (p.Arg534Gln). NM_000130.4(F5):c.3980A>G (p.His1327Arg). NM_000129.3(F13A1):c.103G>T (p.Val35Leu). NM_000212.2(ITGB3):c.176T>C (p.Leu59Pro). NM_000173.7(GP1BA):c.482C>T (p.Thr161Met). NM_000419.5(ITGA2B):c.2621T>G (p.Ile874Ser). NM_000212.2(ITGB3):c.506G>A (p.Arg169Gln). NM_002203.4(ITGA2):c.1600G>A (p.Glu534Lys). NM_000212.2(ITGB3):c.1544G>A (p.Arg515Gln). NM_000602.5(SERPINE1):c.-820G[(4_5)]. NM_005957.5(MTHFR):c.665C>T (p.Ala222Val). NM_005957.4(MTHFR):c.1286A>C (p.Glu429Ala). NM_000789.3(ACE):c.2306-117_2306-116insAF118569.1:g.14094_14382. NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln). NM_000041.2(APOE):c.526C>T (p.Arg176Cys). NM_000041.4(APOE):c.388T>C (p.Cys130Arg). NM_000254.2(MTR):c.2756A>G (p.Asp919Gly). NM_002454.3(MTRR):c.66A>G (p.Ile22Met). NM_000029.4(AGT):c.803T>C (p.Met268Thr). NM_031850.3(AGTR1):c.*86A>C. NM_000852.4(GSTP1):c.313A>G (p.Ile105Val). NM_000506.5(F2):c.*97G>A.
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