rs1800844, PSEN1

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.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 1.000 0.040 14 73136992 5 prime UTR variant G/A;C snv 0.010 1.000 1 2011 2011
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 1.000 0.040 14 73136992 5 prime UTR variant G/A;C snv 0.010 1.000 1 2011 2011