rs104893823, TNNC1

N. diseases: 5
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, Dilated, 1z
CUI: C2678475
Disease: Cardiomyopathy, Dilated, 1z
1 0.882 0.040 3 52451285 missense variant C/T snv 0.700 0
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.882 0.040 3 52451285 missense variant C/T snv 0.040 1.000 4 2007 2016
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.882 0.040 3 52451285 missense variant C/T snv 0.040 1.000 4 2007 2016
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.040 3 52451285 missense variant C/T snv 0.010 1.000 1 2008 2008
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.882 0.040 3 52451285 missense variant C/T snv 0.010 1.000 1 2008 2008