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: rs1294156190
rs1294156190
1.000 0.040 22 19880680 missense variant C/T snv 4.0E-06
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs752863555
rs752863555
1.000 0.040 22 19919597 missense variant C/G;T snv 1.2E-05; 2.4E-05
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs754065483
rs754065483
1.000 0.040 22 19918969 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs754916024
rs754916024
1.000 0.040 22 19878123 missense variant C/T snv 1.2E-05 7.0E-06
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs757239766
rs757239766
1.000 0.040 22 19880681 missense variant C/A;G;T snv 1.6E-05
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2011 2011