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: rs492842
rs492842
5 79114164 intron variant C/T snv 0.59
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs542852
rs542852
5 79113573 intron variant T/C snv 0.63
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2017 2017