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: rs3732378
rs3732378
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12
CUI: C0243050
Disease: Cardiovascular Abnormalities
Cardiovascular Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2003 2003
dbSNP: rs3732379
rs3732379
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22
CUI: C0243050
Disease: Cardiovascular Abnormalities
Cardiovascular Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2003 2003