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: rs104894580
rs104894580
0.790 0.240 17 70175238 missense variant C/A;T snv 4.0E-06
Ventricular tachycardia, polymorphic
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs199473374
rs199473374
1.000 0.080 17 70175340 missense variant T/C snv
Ventricular tachycardia, polymorphic
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2004 2004