RS797044887 PDGFRB

Health Risk Chr 5:150124277
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Acroosteolysis-keloid-like lesions-premature aging syndrome
Basal ganglia calcification
idiopathic
4
Infantile myofibromatosis
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome
Inborn genetic diseases
Acroosteolysis-keloid-like lesions-premature aging syndrome
Basal ganglia calcification
idiopathic
4
Infantile myofibromatosis
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome
Other Variants in PDGFRB
rs397509381 rs367543286 rs138008832 rs759436020 rs863224946 rs1554108211 rs864309711 rs1554108389 rs1060499543 rs1060499541
Ask Dr. Hemsworth about this variant