rs1904589, NODAL

N. diseases: 2
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.
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 1.000 0.040 10 70435683 missense variant T/C snv 0.62 0.56 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 10 70435683 missense variant T/C snv 0.62 0.56 0.010 1.000 1 2013 2013