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 |
rs3218713
|
|
0.763 |
0.160 |
14 |
23431468 |
missense variant
|
C/A;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
42 |
1991 |
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 |
39 |
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 |
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 |
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 |
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 |
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 |
rs3218716
|
|
0.716 |
0.280 |
14 |
23425316 |
missense variant
|
C/A;G;T
|
snv
|
4.0E-06;
2.4E-05
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
32 |
1975 |
2017 |
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 |
rs3218714
|
|
0.763 |
0.160 |
14 |
23429279 |
missense variant
|
G/A;C
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
30 |
1992 |
2017 |
rs397516161
|
|
0.882 |
0.080 |
14 |
23424148 |
missense variant
|
T/A;C
|
snv
|
4.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
30 |
1992 |
2017 |
rs397516269
|
|
0.882 |
0.080 |
14 |
23431426 |
missense variant
|
A/G
|
snv
|
4.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
28 |
1992 |
2017 |
rs141764279
|
|
1.000 |
0.080 |
14 |
23418398 |
missense variant
|
G/A;T
|
snv
|
2.8E-05;
1.1E-04
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.700 |
1.000 |
27 |
1992 |
2017 |
rs397516212
|
|
0.925 |
0.080 |
14 |
23432703 |
missense variant
|
C/A;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
27 |
1992 |
2017 |
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 |
rs267606910
|
|
0.807 |
0.080 |
14 |
23431589 |
missense variant
|
C/T
|
snv
|
8.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
26 |
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 |
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 |
rs121913639
|
|
1.000 |
0.080 |
14 |
23424026 |
missense variant
|
C/T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs397516110
|
|
1.000 |
0.080 |
14 |
23428546 |
missense variant
|
A/G
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs397516157
|
|
0.882 |
0.080 |
14 |
23424893 |
missense variant
|
A/C;G;T
|
snv
|
4.0E-06
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs397516171
|
|
0.763 |
0.160 |
14 |
23424041 |
missense variant
|
C/G;T
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |
rs863225097
|
|
1.000 |
0.080 |
14 |
23425780 |
missense variant
|
T/G
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
0.800 |
1.000 |
25 |
1992 |
2017 |