openSNP | rs2359612

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Note: For some SNPs, testing providers detect the genotype from the opposite strand of DNA, so that the genotypes listed on openSNP don't appear here. In those cases, please replace "A" by "T" or "G" by "C" (and vice-versa).

Publications on this SNP on the Public Library of Science:

First Author	Title	Year of Publication	# of readers
Blandine Patillon	Positive Selection in the Chromosome 16 VKORC1 Genomic Region Has Contributed to the Variability of Anticoagulant Response in Humans	2012	3779
Fumihiko Takeuchi	A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose	2009	27946
Andrea L. Jorgensen	Influence of CYP2C9 and VKORC1 on Patient Response to Warfarin: A Systematic Review and Meta-Analysis	2012	13201
Ramasamy Saminathan	VKORC1 Pharmacogenetics and Pharmacoproteomics in Patients on Warfarin Anticoagulant Therapy: Transthyretin Precursor as a Potential Biomarker	2010	5419
Dana C. Crawford	VKORC1 Common Variation and Bone Mineral Density in the Third National Health and Nutrition Examination Survey	2010	2682

Publications on this SNP on Mendeley

First Author	Title	Pub. Year	# of Readers	DOI
Matthias Watzka	Functional promoter polymorphism in the VKORC1 gene is no major genetic determinant for coronary heart disease in Northern Germans.	2007	5	-
Yibo Wang	VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification.	2013	1	10.1007/s00439-012-1222-y
Ilona Kurnatowska	Epidemiology - cardiovascular outcomes: The effect of Vitamin K2 substitution on atherosclerosis and vascular calcification markers in non-dialyzed patients in chronic kidney disease stage 3-5	2013	1	10.1093/ndt/gft130
Marie-Luise Arnold	Pharmacogenetic testing for guiding de novo phenprocoumon therapy in stroke patients.	2009	6	-
Yibo Wang	VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification.	2013	2	10.1007/s00439-012-1222-y
Marie-Luise Arnold	Pharmacogenetic testing for guiding de novo phenprocoumon therapy in stroke patients.	2009	7	10.1159/000235992
Marie Luise Arnold	Pharmacogenetic testing for guiding de novo phenprocoumon therapy in stroke patients	2009	7	10.1159/000235992
Marie-Luise Arnold	Single nucleotide polymorphisms in the VKORC1 gene and the risk of stroke in the Southern German population.	2008	7	10.1160/TH07-10-0617
刘媛	华法林药代学和药动学通路突变等位基因在中国汉族人群中的分布	2011	1	10.3969/j.issn.1671-167X.2011.06.003
M Watzka	Functional promoter polymorphism in the VKORC1 gene is no major genetic determinant for coronary heart disease in Northern Germans	2007	0	-
Dhakchinamoorthi Krishna Kumar	Effect of CYP2C9, VKORC1, CYP4F2 and GGCX genetic variants on warfarin maintenance dose and explicating a new pharmacogenetic algorithm in South Indian population.	2014	5	10.1007/s00228-013-1581-x
Marie-Luise Arnold	Single nucleotide polymorphisms in the VKORC1 gene and the risk of stroke in the Southern German population.	2008	2	-
Matthias Watzka	Functional promoter polymorphism in the VKORC1 gene is no major genetic determinant for coronary heart disease in Northern Germans.	2007	8	10.1160/TH06-11-0643

Evidence compiled by the Personal Genome Project

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Publications listed by Genome.gov

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Name	rs2359612
Chromosome	16
Position	31092475
Weight of evidence	23

SNP rs2359612

Basic Information

Genotype Frequency

Allele Frequency

Additional Information

Links to SNPedia

Publications on this SNP on the Public Library of Science:

Publications on this SNP on Mendeley

Evidence compiled by the Personal Genome Project

Publications listed by Genome.gov

Users who share this SNP:

Genome Browser

Contacts