rs104893749
|
|
0.925 |
0.080 |
3 |
46859495 |
missense variant
|
C/A;T
|
snv
|
4.0E-06;
2.4E-05
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
2 |
1996 |
2012 |
rs1057517711
|
|
1.000 |
0.080 |
12 |
2566466 |
missense variant
|
G/A
|
snv
|
|
7.0E-06
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1057517771
|
|
1.000 |
0.080 |
14 |
23432656 |
missense variant
|
T/C
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
|
0 |
|
|
rs1057517772
|
|
1.000 |
0.080 |
14 |
23431839 |
missense variant
|
G/A;C
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
|
0 |
|
|
rs121908107
|
|
1.000 |
0.080 |
20 |
31820333 |
missense variant
|
C/T
|
snv
|
1.6E-04
|
1.3E-04
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
1 |
2001 |
2001 |
rs121908108
|
|
1.000 |
0.080 |
20 |
31820357 |
missense variant
|
C/A
|
snv
|
5.8E-04
|
2.0E-03
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
6 |
2001 |
2017 |
rs121909280
|
|
1.000 |
0.080 |
3 |
8745602 |
missense variant
|
C/G
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
6 |
2004 |
2017 |
rs121909374
|
|
0.790 |
0.120 |
11 |
47342578 |
stop gained
|
C/A;G
|
snv
|
1.3E-05
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
24 |
1990 |
2015 |
rs121913624
|
|
0.851 |
0.080 |
14 |
23429278 |
missense variant
|
C/A;G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
76 |
1961 |
2017 |
rs121913625
|
|
0.851 |
0.080 |
14 |
23429005 |
missense variant
|
G/A;C;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
34 |
1990 |
2014 |
rs121913626
|
|
0.882 |
0.080 |
14 |
23427723 |
missense variant
|
C/A;G;T
|
snv
|
4.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
26 |
1992 |
2014 |
rs121913627
|
|
0.851 |
0.080 |
14 |
23427657 |
missense variant
|
C/A;G;T
|
snv
|
4.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
30 |
1992 |
2014 |
rs121913628
|
|
0.763 |
0.160 |
14 |
23424059 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
34 |
1992 |
2017 |
rs121913629
|
|
1.000 |
0.080 |
14 |
23423984 |
missense variant
|
C/T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
25 |
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 |
35 |
1992 |
2017 |
rs121913631
|
|
0.882 |
0.080 |
14 |
23424107 |
missense variant
|
G/C
|
snv
|
|
1.4E-05
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
37 |
1992 |
2017 |
rs121913632
|
|
0.882 |
0.080 |
14 |
23425760 |
missense variant
|
C/A;G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
33 |
1992 |
2017 |
rs121913633
|
|
0.882 |
0.080 |
14 |
23431447 |
missense variant
|
C/T
|
snv
|
|
7.0E-06
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
20 |
1992 |
2005 |
rs121913634
|
|
0.882 |
0.080 |
14 |
23425372 |
missense variant
|
T/A;C
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs121913636
|
|
0.925 |
0.080 |
14 |
23428540 |
missense variant
|
A/C
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs121913637
|
|
0.882 |
0.080 |
14 |
23425971 |
missense variant
|
G/A
|
snv
|
|
7.0E-06
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
50 |
1992 |
2017 |
rs121913638
|
|
0.851 |
0.120 |
14 |
23425980 |
missense variant
|
C/T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
22 |
1992 |
2005 |
rs121913639
|
|
1.000 |
0.080 |
14 |
23424026 |
missense variant
|
C/T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs121913640
|
|
1.000 |
0.080 |
14 |
23429867 |
missense variant
|
A/G
|
snv
|
|
2.1E-05
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
20 |
1992 |
2005 |
rs121913641
|
|
0.882 |
0.080 |
14 |
23425970 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
35 |
1992 |
2017 |