ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.96+15_96+31del

dbSNP: rs730882011
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000161043 SCV000211773 benign Hereditary cancer-predisposing syndrome 2014-01-10 criteria provided, single submitter clinical testing The variant is found in BR-OV-HEREDIC panel(s).
Labcorp Genetics (formerly Invitae), Labcorp RCV002053938 SCV002334440 likely benign Li-Fraumeni syndrome 2022-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000161043 SCV002582300 likely benign Hereditary cancer-predisposing syndrome 2022-06-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002288696 SCV002582962 likely benign Li-Fraumeni syndrome 1 2022-06-18 criteria provided, single submitter clinical testing

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