rs121908601, ZFPM2

N. diseases: 4
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.
Tetralogy of Fallot
CUI: C0039685
Disease: Tetralogy of Fallot
83 0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03 0.700 1.000 2 2003 2011
CONOTRUNCAL HEART MALFORMATIONS (disorder)
22 0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03 0.700 1.000 1 2011 2011
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
45 0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03 0.010 1.000 1 2011 2011
Double Outlet Right Ventricle
CUI: C0013069
Disease: Double Outlet Right Ventricle
16 0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03 0.010 1.000 1 2011 2011