ClinVar Miner

Submissions for variant NM_001126112.2(TP53):c.993+326_993+341del (rs730882013)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000161052 SCV000211782 benign Hereditary cancer-predisposing syndrome 2014-01-27 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,HIRISK-BR-HEREDIC panel(s).
Counsyl RCV000409271 SCV000488730 likely benign Li-Fraumeni syndrome 1 2016-06-02 criteria provided, single submitter clinical testing
Color Health, Inc RCV000161052 SCV000691698 likely benign Hereditary cancer-predisposing syndrome 2015-02-13 criteria provided, single submitter clinical testing

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