Factor V Leiden Mutation Test in Chennai

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5250.0 for Factor V Leiden Mutation
Closed today
Mon
07:30 AM - 07:00 PM
Tue
07:30 AM - 07:00 PM
Wed
07:30 AM - 07:00 PM
Thu
07:30 AM - 07:00 PM
Fri
07:30 AM - 07:00 PM
Sat
07:30 AM - 07:00 PM
Sun
07:30 AM - 12:00 PM

Kilpauk, Chennai
5250.0 for Factor V Leiden Mutation
Closed today
Mon
08:00 AM - 08:00 PM
Tue
08:00 AM - 08:00 PM
Wed
08:00 AM - 08:00 PM
Thu
08:00 AM - 08:00 PM
Fri
08:00 AM - 08:00 PM
Sat
08:00 AM - 08:00 PM
5250.0 for Factor V Leiden Mutation
Closed today
Mon
07:00 AM - 06:00 PM
Tue
07:00 AM - 06:00 PM
Wed
07:00 AM - 06:00 PM
Thu
07:00 AM - 06:00 PM
Fri
07:00 AM - 06:00 PM
Sat
07:00 AM - 06:00 PM
5250.0 for Factor V Leiden Mutation
Closed today
Mon
08:00 AM - 05:00 PM
Tue
08:00 AM - 05:00 PM
Wed
08:00 AM - 05:00 PM
Thu
08:00 AM - 05:00 PM
Fri
08:00 AM - 05:00 PM
Sat
08:00 AM - 05:00 PM
5250.0 for Factor V Leiden Mutation
Closed today
Mon
07:30 AM - 07:30 PM
Tue
07:30 AM - 07:30 PM
Wed
07:30 AM - 07:30 PM
Thu
07:30 AM - 07:30 PM
Fri
07:30 AM - 07:30 PM
Sat
07:30 AM - 07:30 PM
Sun
07:30 AM - 12:00 PM

Home sample pickup available Mogappair East, Chennai
6500.0 for Factor V Leiden Mutation
Closed today
Mon
07:00 AM - 09:00 PM
Tue
10:00 AM - 07:00 PM
Wed
10:00 AM - 07:00 PM
Thu
10:00 AM - 07:00 PM
Fri
10:00 AM - 07:00 PM
Sat
10:00 AM - 07:00 PM
Sun
12:00 AM - 01:00 PM
Sorry! Your search did not match any lab. Please contact Lybrate's helpline: +91-901-555-9900.
About Factor V Leiden Mutation Test

Factor-V-Leiden-alteration cause unsuitable blood clot (thrombus) formation in veins, a situation called deep vein thrombosis (DVT) and/or venous thromboembolism (VTE). The lab test is ordered to assist in diagnosing the root of it. Factor V and prothrombin are the two coagulation factors that are fundamental to proper blood clot formation. People who have a mutation in one of the genes that code for these factors have an increased risk of blood clots. Testing for Factor V Leiden and PT 20120 mutations is used to help determine if an adult individual has inherited a disorder linked with blood clots and can settle on whether the person has 1 copy or two copies of the change (heterozygous or homozygous.)

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