Disease: Vitamin K Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72547528
rs72547528
Entrez Id: 79001;339105
Gene Symbol: VKORC1;PRSS53
VKORC1;PRSS53
CUI: C0042880
Disease:
Vitamin K Deficiency 		0.010 GeneticVariation BEFREE The second phenotype, a very rare autosomal-recessive bleeding disorder caused by combined deficiency of vitamin K dependent clotting factors type 2 (VKCFD2) arises from a homozygous Arg98Trp mutation. 26287237 2015