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: rs1282433424
rs1282433424
0.925 0.080 8 11755094 missense variant C/T snv
Ostium secundum atrial septal defect
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 0
dbSNP: rs3729856
rs3729856
0.925 0.080 8 11757066 missense variant A/G snv 9.5E-02 9.0E-02
Ostium secundum atrial septal defect
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2011 2011