rs121909298, SGCD

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, DILATED, 1L
CUI: C1847667
Disease: CARDIOMYOPATHY, DILATED, 1L
8 0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 0.700 1.000 1 2000 2000
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 0.020 0.500 2 2009 2014
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 0.010 1.000 1 2014 2014
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 0.010 1.000 1 2014 2014