ClinVar Miner

Submissions for variant NM_002609.4(PDGFRB):c.1579+10C>T

dbSNP: rs571420039
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000878029 SCV001020869 benign Acroosteolysis-keloid-like lesions-premature aging syndrome; Basal ganglia calcification, idiopathic, 4; Infantile myofibromatosis; Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome 2021-10-24 criteria provided, single submitter clinical testing

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