rs397514616, TNNC1

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.
Cardiomyopathy, Familial Hypertrophic, 13
CUI: C2750472
Disease: Cardiomyopathy, Familial Hypertrophic, 13
6 0.851 0.120 3 52452217 missense variant C/A;T snv 0.700 0
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.851 0.120 3 52452217 missense variant C/A;T snv 0.010 1.000 1 2012 2012
Hypertrophic obstructive cardiomyopathy
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
90 0.851 0.120 3 52452217 missense variant C/A;T snv 0.010 1.000 1 2012 2012
Ventricular Fibrillation
CUI: C0042510
Disease: Ventricular Fibrillation
19 0.851 0.120 3 52452217 missense variant C/A;T snv 0.010 1.000 1 2012 2012