ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.74+50_74+55dup

dbSNP: rs2073512697
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001175835 SCV001339604 likely benign Hereditary cancer-predisposing syndrome 2016-04-19 criteria provided, single submitter clinical testing
Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C. RCV001175835 SCV004014905 likely benign Hereditary cancer-predisposing syndrome 2023-07-19 criteria provided, single submitter clinical testing

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