Upload the DNA data file of the test

23andMe, AncestryDNA, FamilyTreeDNA, MyHeritage

and get an enhanced
personalized health report
free without registration

Files accepted .txt, .csv, .zip, .csv.gz

File data is not stored on the server

SNP information rs699664

RS699664

Normal allele: CC

Polymorphism rs699664 is related to topics like this:

Factor 5 blood clotting disorder

Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...


Research and publications:

  17029979   A functional single nucleotide polymorphism in the vitamin-K-dependent gamma-glutamyl carboxylase gene (Arg325Gln) is associated with bone mineral density in elderly Japanese women.

  18574025   The largest prospective warfarin-treated cohort supports genetic forecasting

  19436136   Association of sequence variations in vitamin K epoxide reductase and gamma-glutamyl carboxylase genes with biochemical measures of vitamin K status.

  20149073   Pharmacogenetics of acenocoumarol in patients with extreme dose requirements.

  20615890   A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk.

  20694283   Gamma-glutamyl carboxylase and its influence on warfarin dose.

  20716240   New genetic variant that might improve warfarin dose prediction in African Americans.

  21628633   Circulating uncarboxylated matrix gla protein is associated with vitamin K nutritional status, but not coronary artery calcium, in older adults.

  22158446   Association of the GGCX (CAA)16/17 repeat polymorphism with higher warfarin dose requirements in African Americans.

  22178823   [Distribution of variant alleles association with warfarin pharmacokinetics and pharmacodynamics in the Han population in China].

  22329724   Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.

  22676711   Pharmacogenomics of warfarin in populations of African descent.

  23941071   Association of genetic polymorphisms with warfarin dose requirements in Chinese patients.

  24944790   Screening for 392 polymorphisms in 141 pharmacogenes.

  25126975   A pharmacogenetics-based warfarin maintenance dosing algorithm from Northern Chinese patients.

  25594941   Warfarin dosage response related pharmacogenetics in Chinese population.

  25681132   Impact of gamma-glutamyl carboxylase gene polymorphisms on warfarin dose requirement: a systematic review and meta-analysis.

  26106580   Impact of polymorphisms of the GGCX gene on maintenance warfarin dose in Chinese populations: Systematic review and meta-analysis.

  26979803   Chromatin interactions and candidate genes at ten prostate cancer risk loci.

  27262824   Effect of VKORC1, CYP2C9, CFP4F2, and GGCX Gene Polymorphisms on Warfarin Dose in Japanese Pediatric Patients.

  27632229   Genetic determinants of variability in warfarin response after the dose-titration phase.

  28049362   Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.

  28429387   The association between GGCX, miR-133 genetic polymorphisms and warfarin stable dosage in Han Chinese patients with mechanical heart valve replacement.

  30981116   Vitamin K2-Dependent GGCX and MGP Are Required for Homeostatic Calcium Regulation of Sperm Maturation.

  31854268   Impact of CYP2C9, VKORC1, ApoE and ABCB1 polymorphisms on stable warfarin dose requirements in elderly Chinese patients.

  32380173   Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists.

  35866816   Impact of VKORC1, CYP2C9, CYP1A2, UGT1A1, and GGCX polymorphisms on warfarin maintenance dose: Exploring a new algorithm in South Chinese patients accept mechanical heart valve replacement.

Memory genes

Despite being often overlooked, the brain possesses an impressive ability to restrict the creation...

Genetics and high blood pressure

Abnormally high blood pressure in the arteries, which transport blood from the heart to the rest of...

G20210A prothrombin mutation

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

en
|
de
|
fr
|
es
|
it
|
ua
|
ru

Support