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: rs34376731
rs34376731 		0.925 0.040 12 54581014 missense variant C/T snv 4.6E-03 1.9E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.020 1.000 2 2008 2009
dbSNP: rs34376731
rs34376731 		0.925 0.040 12 54581014 missense variant C/T snv 4.6E-03 1.9E-02
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.020 1.000 2 2008 2009
dbSNP: rs1249958
rs1249958 		0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1249958
rs1249958 		0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1249958
rs1249958 		0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1318306893
rs1318306893 		1.000 0.040 12 54588436 missense variant T/A snv 9.1E-06
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2017 2017