RS1060499542 PDGFRB
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What This Variant Does
"CLNSIG=5
Associated Conditions
Infantile myofibromatosis
Inborn genetic diseases
Hydrocephalus
Myofibromatosis
infantile
1
Dandy-Walker syndrome
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome
Acroosteolysis-keloid-like lesions-premature aging syndrome
Basal ganglia calcification
idiopathic
4
Infantile myofibromatosis
Inborn genetic diseases
Hydrocephalus
Other Variants in PDGFRB