Biomarker Lens

Biomarkers · Chemical

Prothrombin Factor II 20210GA Mutation Analysis

What it measures

Also listed as
na, plasma sodium, Prothrombin (Factor II) 20210G→A Mutation Analysis, serum sodium
Tests in the graph that measure it
8

A plain-language description with its source has not been added for this biomarker yet. What the laboratories say about the tests that measure it is below.

Tests that measure Prothrombin Factor II 20210GA Mutation Analysis

Venous Thrombosis Hypercoagulability Panel with Reflex and Consultation

Laboratory
Quest Diagnostics
Test code
19656
Specimen
Serum
Fasting
Not stated as required

What the laboratory says this test is for

This panel evaluates for the most common hereditary and acquired venous thrombophilia risk factors.

Quest Diagnostics test directory, test code 19656

Recurrent Miscarriage EvaluationCoagulation Panel with Consultation

Laboratory
Quest Diagnostics
Test code
19671
Specimen
Serum
Fasting
Not stated as required

Quest Diagnostics test directory, test code 19671

Thrombophilia Screen II Inherited

Laboratory
Quest Diagnostics
Test code
11327
Specimen
Plasma
Fasting
Not stated as required

What the laboratory says this test is for

Factor V Leiden (R506Q) is the most common genetic determinant for hereditary venous thrombosis. Another DNA variant, the HR2 allele, has been associated with a 3-4 fold increased risk to venous thrombosis when it occurs in the presence of the Factor V Leiden mutation.

Quest Diagnostics test directory, test code 11327

Prothrombin Factor II 20210GA Mutation Analysis

Laboratory
Quest Diagnostics
Test code
17909
Specimen
Blood
Fasting
Not stated as required

What the laboratory says this test is for

Factor II Mutation (G20210A) is one of the most common causes of venous thrombosis. 2.3% of the general population is heterozygous in contrast with 6.2% of patients with venous thrombosis and 18% with familial venous thrombosis. Other risk factors compound the risk for venous thrombosis.

Quest Diagnostics test directory, test code 17909

Venous Thrombosis Hypercoag Panel wReflex Consultation Warfarin Patient

Laboratory
Quest Diagnostics
Test code
19655
Specimen
Serum
Fasting
Not stated as required

What the laboratory says this test is for

This panel evaluates for the most common hereditary and acquired venous thrombophilia risk factors except for Protein C and S.

Quest Diagnostics test directory, test code 19655

Recurrent MiscarriageCoagulation Panel with Reflex without Consultation

Laboratory
Quest Diagnostics
Test code
11469
Specimen
Plasma
Fasting
Not stated as required

What the laboratory says this test is for

This profile examines the most common hereditary and acquired thrombophilia risk factors associated with recurrent miscarriage or stillbirth.

Quest Diagnostics test directory, test code 11469

Venous Thrombosis Hypercoagulability Panel with Reflex

Laboratory
Quest Diagnostics
Test code
11475
Specimen
Plasma
Fasting
Not stated as required

What the laboratory says this test is for

This panel evaluates for the most common hereditary and acquired venous thrombophilia risk factors.

Quest Diagnostics test directory, test code 11475

Venous Thrombosis Hypercoagulability Panel with Reflex Warfarin Patient

Laboratory
Quest Diagnostics
Test code
11472
Specimen
Plasma
Fasting
Not stated as required

What the laboratory says this test is for

This panel evaluates for the most common hereditary and acquired venous thrombophilia risk factors except for Protein C and S.

Quest Diagnostics test directory, test code 11472

About this page

Everything above is drawn from the named sources and shown as they published it. Reference ranges belong to the laboratory that issued them and the population it named; they are not a universal normal. This page describes the biomarker in general and does not interpret anyone's result. For your own numbers, talk to a clinician, or use Aumnivida, which reads the same graph next to your records.

Found an error? Write to hello@biomarkerlens.com with the page link and the source that contradicts it.