rs116840778
|
0.882 |
0.200 |
3 |
8733956 |
missense variant |
G/A;C
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
14 |
2000 |
2011 |
rs116840778
|
0.882 |
0.200 |
3 |
8733956 |
missense variant |
G/A;C
|
snv
|
|
|
RIPPLING MUSCLE DISEASE 2 (disorder)
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.800 |
1.000 |
14 |
2000 |
2011 |
rs116840805
|
0.827 |
0.160 |
3 |
8745725 |
missense variant |
C/T
|
snv
|
|
|
RIPPLING MUSCLE DISEASE 2 (disorder)
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.800 |
1.000 |
12 |
1998 |
2006 |
rs199476332
|
0.925 |
0.120 |
3 |
8745601 |
missense variant |
A/C
|
snv
|
|
|
RIPPLING MUSCLE DISEASE 2 (disorder)
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.700 |
1.000 |
12 |
1998 |
2006 |
rs121909280
|
1.000 |
0.080 |
3 |
8745602 |
missense variant |
C/G
|
snv
|
|
|
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
2004 |
2017 |
rs104893714
|
0.925 |
0.120 |
3 |
8745701 |
missense variant |
T/G
|
snv
|
|
|
LONG QT SYNDROME 9 (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.820 |
1.000 |
4 |
2006 |
2018 |
rs28936686
|
0.851 |
0.200 |
3 |
8745688 |
missense variant |
G/A;T
|
snv
|
1.6E-04;
2.0E-05
|
|
Rippling muscle disease
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.700 |
1.000 |
3 |
2003 |
2010 |
rs104893713
|
1.000 |
0.120 |
3 |
8745834 |
missense variant |
C/G
|
snv
|
8.0E-06
|
|
LONG QT SYNDROME 9 (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
2 |
2006 |
2007 |
rs104893715
|
1.000 |
0.120 |
3 |
8745664 |
missense variant |
G/A
|
snv
|
|
|
LONG QT SYNDROME 9 (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
2 |
2006 |
2007 |
rs116840805
|
0.827 |
0.160 |
3 |
8745725 |
missense variant |
C/T
|
snv
|
|
|
Muscular Dystrophies, Limb-Girdle
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
0.020 |
1.000 |
2 |
2004 |
2008 |
rs116840805
|
0.827 |
0.160 |
3 |
8745725 |
missense variant |
C/T
|
snv
|
|
|
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
0.020 |
1.000 |
2 |
2004 |
2019 |
rs28936686
|
0.851 |
0.200 |
3 |
8745688 |
missense variant |
G/A;T
|
snv
|
1.6E-04;
2.0E-05
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
2 |
2003 |
2005 |
rs72546668
|
0.807 |
0.200 |
3 |
8745644 |
missense variant |
C/A;T
|
snv
|
4.0E-06;
2.6E-03
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.020 |
0.500 |
2 |
2013 |
2017 |
rs1008642
|
0.882 |
0.120 |
3 |
8733975 |
missense variant |
C/A;G;T
|
snv
|
0.29
|
|
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs104893714
|
0.925 |
0.120 |
3 |
8745701 |
missense variant |
T/G
|
snv
|
|
|
Cardiac Arrhythmia
|
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs104893714
|
0.925 |
0.120 |
3 |
8745701 |
missense variant |
T/G
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs116840773
|
0.925 |
0.080 |
3 |
8745548 |
missense variant |
C/A;T
|
snv
|
|
|
Rippling muscle disease
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs116840778
|
0.882 |
0.200 |
3 |
8733956 |
missense variant |
G/A;C
|
snv
|
|
|
Peripheral Nervous System Diseases
|
Nervous System Diseases
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs116840778
|
0.882 |
0.200 |
3 |
8733956 |
missense variant |
G/A;C
|
snv
|
|
|
Peripheral Neuropathy
|
Nervous System Diseases
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs116840778
|
0.882 |
0.200 |
3 |
8733956 |
missense variant |
G/A;C
|
snv
|
|
|
Muscular Dystrophies, Limb-Girdle
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2003 |
2003 |
rs116840782
|
0.925 |
0.080 |
3 |
8733960 |
missense variant |
C/A
|
snv
|
|
|
Rippling muscle disease
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs116840788
|
0.925 |
0.120 |
3 |
8745542 |
missense variant |
T/A;C
|
snv
|
4.0E-06
|
|
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs116840789
|
0.925 |
0.080 |
3 |
8745547 |
missense variant |
G/A;T
|
snv
|
|
|
Rippling muscle disease
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs116840789
|
0.925 |
0.080 |
3 |
8745547 |
missense variant |
G/A;T
|
snv
|
|
|
Myalgia
|
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs116840789
|
0.925 |
0.080 |
3 |
8745547 |
missense variant |
G/A;T
|
snv
|
|
|
Muscle Cramp
|
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2000 |
2000 |