Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894503
rs104894503
0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05
Cardiomyopathy, Hypertrophic, Familial
0.740 1.000 12 1994 2015
dbSNP: rs104894724
rs104894724
0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.730 1.000 14 1997 2017
dbSNP: rs368861241
rs368861241
0.851 0.120 19 55154095 missense variant G/A snv 4.0E-05 7.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.720 1.000 14 1997 2017
dbSNP: rs371898076
rs371898076
0.763 0.160 14 23426833 missense variant C/T snv 8.0E-06 4.9E-05
Cardiomyopathy, Hypertrophic, Familial
0.710 1.000 17 1999 2016
dbSNP: rs36211715
rs36211715
0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.710 1.000 16 1995 2017
dbSNP: rs121913624
rs121913624
0.851 0.080 14 23429278 missense variant C/A;G;T snv
Cardiomyopathy, Hypertrophic, Familial
0.710 1.000 13 1990 2018
dbSNP: rs121913630
rs121913630
0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05
Cardiomyopathy, Hypertrophic, Familial
0.710 1.000 12 1992 2018
dbSNP: rs3218713
rs3218713
0.763 0.160 14 23431468 missense variant C/A;T snv
Cardiomyopathy, Hypertrophic, Familial
0.710 1.000 5 1991 2015
dbSNP: rs727504245
rs727504245
0.851 0.080 1 201365261 missense variant G/A snv 1.6E-05 2.1E-05
Cardiomyopathy, Hypertrophic, Familial
0.710 1.000 0 1997 1997
dbSNP: rs121913625
rs121913625
0.851 0.080 14 23429005 missense variant G/A;C;T snv
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 19 1992 2014
dbSNP: rs121913632
rs121913632
0.882 0.080 14 23425760 missense variant C/A;G;T snv
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 19 1985 2017
dbSNP: rs397516074
rs397516074
0.827 0.120 11 47348424 missense variant C/T snv 1.7E-05 4.2E-05
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 19 1998 2014
dbSNP: rs121913626
rs121913626
0.882 0.080 14 23427723 missense variant C/A;G;T snv 4.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 17 1992 2018
dbSNP: rs121913631
rs121913631
0.882 0.080 14 23424107 missense variant G/C snv 1.4E-05
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 17 1992 2017
dbSNP: rs397516354
rs397516354
0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 17 1997 2017
dbSNP: rs138049878
rs138049878
0.925 0.080 14 23424840 missense variant G/A snv 2.4E-05 7.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 16 1995 2018
dbSNP: rs202141173
rs202141173
0.882 0.080 14 23424842 missense variant C/T snv 2.4E-05 9.1E-05
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 16 2004 2019
dbSNP: rs397516209
rs397516209
0.882 0.080 14 23432713 missense variant C/T snv 4.0E-06 7.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 16 2001 2016
dbSNP: rs121913627
rs121913627
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 15 1992 2014
dbSNP: rs397515905
rs397515905
0.851 0.080 11 47342719 missense variant G/A;C;T snv 4.0E-06; 8.0E-06
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 15 1998 2017
dbSNP: rs397516127
rs397516127
0.763 0.160 14 23426834 missense variant G/A;C snv
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 14 1999 2019
dbSNP: rs121913638
rs121913638
0.851 0.120 14 23425980 missense variant C/T snv
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 13 1994 2017
dbSNP: rs121913641
rs121913641
0.882 0.080 14 23425970 missense variant C/G;T snv
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 13 1994 2013
dbSNP: rs200411226
rs200411226
0.851 0.080 11 47342718 missense variant C/T snv 2.4E-05 4.2E-05
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 13 1998 2013
dbSNP: rs397516068
rs397516068
0.882 0.080 11 47348541 missense variant C/A;G snv 4.1E-06
Cardiomyopathy, Hypertrophic, Familial
0.700 1.000 12 2004 2017