Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs376344575
rs376344575
0.925 0.040 15 41394885 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.8E-05
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs387906958
rs387906958
0.925 0.040 15 41394987 missense variant G/A snv 3.2E-05 4.2E-05
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
Cardiovascular Diseases 0.010 1.000 1 2011 2011