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: rs1060500609
rs1060500609
1.000 0.080 6 7569185 splice acceptor variant G/T snv
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 0