rs764328696, TBX20

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 1.000 7 35248696 missense variant C/G;T snv 0.010 1.000 1 2014 2014
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 1.000 7 35248696 missense variant C/G;T snv 0.010 1.000 1 2014 2014
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 1.000 7 35248696 missense variant C/G;T snv 0.010 1.000 1 2014 2014