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 RESTRICTIVE, 1 (disorder)
24 0.925 0.040 16 29813487 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.010 1.000 1 2016 2016
Restrictive cardiomyopathy
CUI: C0007196
Disease: Restrictive cardiomyopathy
30 0.925 0.040 16 29813487 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.010 1.000 1 2016 2016