rs104894369
|
0.807 |
0.080 |
12 |
110914287 |
missense variant |
C/A;T
|
snv
|
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
19 |
1996 |
2017 |
rs104894368
|
0.882 |
0.080 |
12 |
110919133 |
stop gained |
C/A;G;T
|
snv
|
4.0E-06;
8.0E-06;
2.0E-05
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
16 |
1996 |
2017 |
rs104894370
|
1.000 |
0.080 |
12 |
110919145 |
missense variant |
A/G
|
snv
|
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
10 |
1996 |
2017 |
rs121913658
|
1.000 |
0.080 |
12 |
110913316 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
10 |
1996 |
2017 |
rs104894363
|
1.000 |
0.080 |
12 |
110919160 |
missense variant |
C/T
|
snv
|
3.7E-04
|
2.0E-04
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
6 |
1996 |
2003 |
rs199474815
|
0.925 |
0.080 |
12 |
110911081 |
missense variant |
T/A
|
snv
|
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
1996 |
2003 |
rs199474813
|
1.000 |
0.080 |
12 |
110911176 |
splice acceptor variant |
C/A;G;T
|
snv
|
4.0E-06;
4.8E-05;
4.0E-06
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
3 |
2001 |
2016 |
rs587782965
|
0.882 |
0.080 |
12 |
110914221 |
missense variant |
G/T
|
snv
|
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
3 |
2011 |
2017 |
rs397516407
|
0.925 |
0.080 |
12 |
110911090 |
missense variant |
T/C;G
|
snv
|
|
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
2 |
2011 |
2014 |
rs143139258
|
0.882 |
0.080 |
12 |
110913097 |
missense variant |
T/G
|
snv
|
2.0E-04
|
2.9E-04
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs863225117
|
1.000 |
0.080 |
12 |
110915759 |
missense variant |
C/T
|
snv
|
|
7.0E-06
|
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|