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SNP information rs7080536

RS7080536

Normal allele: GG

Polymorphism rs7080536 is related to topics like this:

G20210A prothrombin mutation

The Prothrombin G20210A mutation, also known as Factor II mutation, is a hereditary trait that...


Research and publications:

  12138371   The frequent Marburg I polymorphism impairs the pro-urokinase activating potency of the factor VII activating protease (FSAP).

  12578864   Marburg I polymorphism of factor VII--activating protease: a prominent risk predictor of carotid stenosis.

  15486068   Marburg I polymorphism of factor VII-activating protease is associated with idiopathic venous thromboembolism.

  19657367   Genetic polymorphisms of EPHX1, Gsk3beta, TNFSF8 and myeloma cell DKK-1 expression linked to bone disease in myeloma.

  21935354   Phased whole-genome genetic risk in a family quartet using a major allele reference sequence.

  22421107   The G534E-polymorphism of the gene encoding the factor VII-activating protease is a risk factor for venous thrombosis and recurrent events.

  24365473   An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation.

  26222560   Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer.

  26581002   HABP2 Mutation and Nonmedullary Thyroid Cancer.

  26581003   HABP2 Mutation and Nonmedullary Thyroid Cancer.

  26581004   HABP2 Mutation and Nonmedullary Thyroid Cancer.

  26581005   HABP2 Mutation and Nonmedullary Thyroid Cancer.

  26691890   The HABP2 G534E variant is an unlikely cause of familial non-medullary thyroid cancer.

  26745718   HABP2 G534E Variant in Papillary Thyroid Carcinoma.

  27097599   The HABP2 G534E polymorphism does not increase nonmedullary thyroid cancer risk in Hispanics.

  28884020   Pitfalls of exome sequencing: a case study of the attribution of HABP2 rs7080536 in familial non-medullary thyroid cancer.

  30070759   Genome-wide analysis of genetic determinants of circulating factor VII-activating protease (FSAP) activity.

  30143058   Hyaluronan-binding protein 2 (HABP2) gene variation in women with recurrent miscarriage.

  32695137   Workflow for the Implementation of Precision Genomics in Healthcare.

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