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: rs397514520
rs397514520
1.000 0.080 8 105788866 missense variant T/G snv
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 0
dbSNP: rs397514521
rs397514521
1.000 0.080 8 105802291 missense variant A/G snv
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 0
dbSNP: rs121908601
rs121908601
0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs187043152
rs187043152
0.851 0.080 8 105801714 missense variant G/A;T snv 3.4E-03; 4.0E-06
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs202204708
rs202204708
0.882 0.080 8 105788864 missense variant A/G snv 4.5E-04 4.7E-04
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2011 2011