ClinVar Miner

Variants studied for Clubfoot; Coarctation of aorta; Tetralogy of Fallot; Skeletal dysplasia; Atrial septal defect; Toe syndactyly; Scoliosis; Tall stature; Abnormality of the vertebral column; Complete atrioventricular canal defect; Flexion contracture; Arrhythmia; Preaxial polydactyly; Congenital diaphragmatic hernia; Cutis laxa; Hyperextensible skin; Soft skin; Bruising susceptibility; Atrophic scars; Hand oligodactyly; Hyperextensibility of the finger joints; Joint hypermobility; Bilateral talipes equinovarus; Camptodactyly of toe; Foot oligodactyly; Increased susceptibility to fractures; Joint hyperflexibility; Hyperextensible thumb; Finger syndactyly; Lower limb undergrowth; Upper limb undergrowth; Hyperextensibility at elbow; Hyperextensibility of the knee; 4-5 finger syndactyly; Edema of the dorsum of feet; Camptodactyly of finger; Ventricular septal defect; Postaxial polydactyly

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
0 0 0 0 0 0

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