rs17708472, VKORC1

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
WARFARIN SENSITIVITY (disorder)
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
0.010 GeneticVariation BEFREE This study confirmed a genetic association of the <i>CYP2C9</i>*3 and <i>VKORC1</i> rs10871454, rs8050894, rs9934438, and rs17708472 SNPs with warfarin sensitivity. 30486437 2018