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: rs3999950
rs3999950
7 35212128 intron variant C/T snv
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs764328696
rs764328696
1.000 7 35248696 missense variant C/G;T snv
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2014 2014