rs3218713
|
|
0.763 |
0.160 |
14 |
23431468 |
missense variant
|
C/A;T
|
snv
|
|
|
Hypertrophic Cardiomyopathy
|
0.700 |
1.000 |
15 |
1991 |
2017 |
rs371898076
|
|
0.763 |
0.160 |
14 |
23426833 |
missense variant
|
C/T
|
snv
|
8.0E-06
|
4.9E-05
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
15 |
1992 |
2017 |
rs397516127
|
|
0.763 |
0.160 |
14 |
23426834 |
missense variant
|
G/A;C
|
snv
|
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
14 |
1999 |
2019 |
rs727503260
|
|
0.851 |
0.080 |
14 |
23425403 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
14 |
2003 |
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 |
rs121913631
|
|
0.882 |
0.080 |
14 |
23424107 |
missense variant
|
G/C
|
snv
|
|
1.4E-05
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
13 |
1992 |
2017 |
rs121913631
|
|
0.882 |
0.080 |
14 |
23424107 |
missense variant
|
G/C
|
snv
|
|
1.4E-05
|
Hypertrophic Cardiomyopathy
|
0.720 |
1.000 |
13 |
1992 |
2017 |
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
|
|
|
Hypertrophic Cardiomyopathy
|
0.710 |
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 |
rs121913641
|
|
0.882 |
0.080 |
14 |
23425970 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
13 |
1992 |
2017 |
rs36211715
|
|
0.851 |
0.080 |
14 |
23424839 |
missense variant
|
C/A;G;T
|
snv
|
4.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
13 |
1992 |
2017 |
rs397516209
|
|
0.882 |
0.080 |
14 |
23432713 |
missense variant
|
C/T
|
snv
|
4.0E-06
|
7.0E-06
|
Hypertrophic Cardiomyopathy
|
0.700 |
1.000 |
13 |
2001 |
2017 |
rs121913625
|
|
0.851 |
0.080 |
14 |
23429005 |
missense variant
|
G/A;C;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
12 |
1990 |
2014 |
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 |
rs121913638
|
|
0.851 |
0.120 |
14 |
23425980 |
missense variant
|
C/T
|
snv
|
|
|
Hypertrophic Cardiomyopathy
|
0.700 |
1.000 |
12 |
1994 |
2017 |
rs2754158
|
|
0.882 |
0.080 |
14 |
23424876 |
missense variant
|
G/A;C;T
|
snv
|
1.2E-05
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
12 |
2004 |
2017 |
rs397516201
|
|
0.882 |
0.080 |
14 |
23418249 |
missense variant
|
G/A
|
snv
|
4.0E-06
|
1.4E-05
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
12 |
2003 |
2017 |
rs121913628
|
|
0.763 |
0.160 |
14 |
23424059 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
11 |
1992 |
2017 |
rs121913630
|
|
0.851 |
0.080 |
14 |
23425814 |
missense variant
|
G/A;C
|
snv
|
1.2E-05
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
11 |
1992 |
2017 |
rs397516209
|
|
0.882 |
0.080 |
14 |
23432713 |
missense variant
|
C/T
|
snv
|
4.0E-06
|
7.0E-06
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
11 |
1992 |
2017 |
rs45544633
|
|
1.000 |
0.080 |
14 |
23417174 |
missense variant
|
G/A
|
snv
|
|
|
Cardiomyopathy, Dilated
|
0.700 |
1.000 |
11 |
2004 |
2015 |
rs727503278
|
|
0.882 |
0.080 |
14 |
23432714 |
missense variant
|
G/A;C;T
|
snv
|
2.8E-05
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
11 |
2003 |
2015 |
rs727503278
|
|
0.882 |
0.080 |
14 |
23432714 |
missense variant
|
G/A;C;T
|
snv
|
2.8E-05
|
|
Cardiomyopathy, Hypertrophic, Familial
|
0.700 |
1.000 |
11 |
2001 |
2017 |
rs121913632
|
|
0.882 |
0.080 |
14 |
23425760 |
missense variant
|
C/A;G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
10 |
1992 |
2017 |