rs143978652, MYH6

N. diseases: 6
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, 1EE
CUI: C2750466
Disease: Cardiomyopathy, Dilated, 1EE
4 0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 0.800 1.000 1 2005 2005
Cardiomyopathy, Familial Hypertrophic, 14
CUI: C2750467
Disease: Cardiomyopathy, Familial Hypertrophic, 14
3 0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 0.700 0
Sudden Cardiac Death
CUI: C0085298
Disease: Sudden Cardiac Death
40 0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 0.700 0
Wolff-Parkinson-White Syndrome
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
22 0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 0.700 0
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 0.010 1.000 1 2011 2011
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 0.010 1.000 1 2011 2011