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 |
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 |
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 |
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 |
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 |
rs121913624
|
|
0.851 |
0.080 |
14 |
23429278 |
missense variant
|
C/A;G;T
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.710 |
1.000 |
13 |
1990 |
2018 |
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 |
rs3218713
|
|
0.763 |
0.160 |
14 |
23431468 |
missense variant
|
C/A;T
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.710 |
1.000 |
5 |
1991 |
2015 |
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 |
rs121913625
|
|
0.851 |
0.080 |
14 |
23429005 |
missense variant
|
G/A;C;T
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
19 |
1992 |
2014 |
rs121913632
|
|
0.882 |
0.080 |
14 |
23425760 |
missense variant
|
C/A;G;T
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
19 |
1985 |
2017 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
rs397516127
|
|
0.763 |
0.160 |
14 |
23426834 |
missense variant
|
G/A;C
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
14 |
1999 |
2019 |
rs121913638
|
|
0.851 |
0.120 |
14 |
23425980 |
missense variant
|
C/T
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
13 |
1994 |
2017 |
rs121913641
|
|
0.882 |
0.080 |
14 |
23425970 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
13 |
1994 |
2013 |
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 |
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 |