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: rs121908991
rs121908991
0.807 0.120 7 151560610 missense variant C/A;T snv
Hypertrophic obstructive cardiomyopathy
Cardiovascular Diseases 0.020 1.000 2 2005 2007
dbSNP: rs121908989
rs121908989
0.882 0.080 7 151564199 missense variant T/A;C snv 4.0E-06
Hypertrophic obstructive cardiomyopathy
Cardiovascular Diseases 0.010 < 0.001 1 2002 2002
dbSNP: rs267606979
rs267606979
0.882 0.080 7 151560560 missense variant A/G snv
Hypertrophic obstructive cardiomyopathy
Cardiovascular Diseases 0.010 1.000 1 2006 2006