rs3729843, TNNT2

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 0.925 0.040 1 201367856 intron variant C/A;G;T snv 1.8E-04; 0.42 0.020 1.000 2 2013 2014
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.925 0.040 1 201367856 intron variant C/A;G;T snv 1.8E-04; 0.42 0.010 1.000 1 2012 2012