Disease: Brugada Syndrome 7 ×
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: rs587777556
rs587777556 		0.925 0.120 11 123642502 missense variant G/A;T snv 8.0E-06; 4.0E-06
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 2 2010 2011
dbSNP: rs587777557
rs587777557 		0.925 0.080 11 123638288 missense variant A/G snv 4.0E-06
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 2 2010 2011
dbSNP: rs587777558
rs587777558 		0.925 0.080 11 123653785 missense variant C/T snv
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 2 2010 2011
dbSNP: rs121918282
rs121918282 		0.882 0.080 11 123653773 missense variant A/G snv 2.0E-04 3.5E-04
CUI: C2751088
Disease: Brugada Syndrome 7
Brugada Syndrome 7 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 0