rs878854378, TTN;TTN-AS1

N. diseases: 33
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Syncope
CUI: C0039070
Disease: Syncope
0.700 GeneticVariation CLINVAR
Myopia
CUI: C0027092
Disease: Myopia
0.700 GeneticVariation CLINVAR
EMG: myopathic abnormalities
CUI: C4021726
Disease: EMG: myopathic abnormalities
0.700 GeneticVariation CLINVAR
Absent reflex
CUI: C0234146
Disease: Absent reflex
0.700 GeneticVariation CLINVAR
Congenital torticollis
CUI: C0079352
Disease: Congenital torticollis
0.700 GeneticVariation CLINVAR
Atrial Flutter
CUI: C0004239
Disease: Atrial Flutter
0.700 GeneticVariation CLINVAR
Decreased muscle mass
CUI: C1837108
Disease: Decreased muscle mass
0.700 GeneticVariation CLINVAR
Myopathy
CUI: C0026848
Disease: Myopathy
0.700 GeneticVariation CLINVAR
Scapular muscle atrophy
CUI: C3805969
Disease: Scapular muscle atrophy
0.700 GeneticVariation CLINVAR
Down-sloping shoulders
CUI: C1856872
Disease: Down-sloping shoulders
0.700 GeneticVariation CLINVAR
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
CUI: C1837342
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
0.700 GeneticVariation CLINVAR
Slowed saccades
CUI: C1321329
Disease: Slowed saccades
0.700 GeneticVariation CLINVAR
Left-Sided Heart Failure
CUI: C0023212
Disease: Left-Sided Heart Failure
0.700 GeneticVariation CLINVAR
Left ventricular noncompaction cardiomyopathy
CUI: C4021133
Disease: Left ventricular noncompaction cardiomyopathy
0.700 GeneticVariation CLINVAR
Respiratory Depression
CUI: C0235063
Disease: Respiratory Depression
0.700 GeneticVariation CLINVAR
Neonatal respiratory distress
CUI: C4281993
Disease: Neonatal respiratory distress
0.700 GeneticVariation CLINVAR
Asymmetry of the thorax
CUI: C1858033
Disease: Asymmetry of the thorax
0.700 GeneticVariation CLINVAR
Neck webbing
CUI: C0221217
Disease: Neck webbing
0.700 GeneticVariation CLINVAR
Reduced muscle collagen VI
CUI: C4021054
Disease: Reduced muscle collagen VI
0.700 GeneticVariation CLINVAR
Gait imbalance
CUI: C1836150
Disease: Gait imbalance
0.700 GeneticVariation CLINVAR
Shoulder girdle weakness
CUI: C0427063
Disease: Shoulder girdle weakness
0.700 GeneticVariation CLINVAR
Abnormal eyelid morphology
CUI: C4021803
Disease: Abnormal eyelid morphology
0.700 GeneticVariation CLINVAR
Restrictive ventilatory defect
CUI: C3277226
Disease: Restrictive ventilatory defect
0.700 GeneticVariation CLINVAR
Muscle Weakness Upper Limb
CUI: C1698196
Disease: Muscle Weakness Upper Limb
0.700 GeneticVariation CLINVAR
Reflex, Ankle, Absent
CUI: C0558845
Disease: Reflex, Ankle, Absent
0.700 GeneticVariation CLINVAR