Disease: Coumarin Resistance ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894539
rs104894539 		16 31094645 missense variant C/A snv 4.3E-06 1.4E-05
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.800 1.000 2 2004 2011
dbSNP: rs104894540
rs104894540 		16 31094596 missense variant A/G snv
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.800 1.000 2 2004 2011
dbSNP: rs104894541
rs104894541 		16 31094558 missense variant T/C snv 4.1E-06
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.800 1.000 2 2004 2011
dbSNP: rs61742245
rs61742245 		16 31094624 missense variant C/A;T snv 2.4E-03
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.720 1.000 4 2004 2018
dbSNP: rs72547529
rs72547529 		16 31093399 missense variant C/T snv 2.0E-04 8.4E-04
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.720 1.000 2 2011 2016
dbSNP: rs104894542
rs104894542 		16 31091243 missense variant A/C snv
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 1.000 2 2004 2011
dbSNP: rs755767348
rs755767348 		16 31093366 missense variant T/A snv 8.0E-06
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs770703948
rs770703948 		16 31094654 missense variant C/A;G;T snv 8.6E-06; 4.3E-06
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 0