ClinVar Miner

Submissions for variant NM_000546.5(TP53):c.74+38C>G (rs1642785)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000250671 SCV000605415 benign not specified 2016-09-16 criteria provided, single submitter clinical testing
Color RCV000580249 SCV000686765 benign Hereditary cancer-predisposing syndrome 2015-03-31 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000250671 SCV000692102 likely benign not specified no assertion criteria provided clinical testing
PreventionGenetics RCV000250671 SCV000305120 benign not specified criteria provided, single submitter clinical testing

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