ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.375+18G>A

dbSNP: rs1567555404
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000776561 SCV000912173 likely benign Hereditary cancer-predisposing syndrome 2017-07-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067334 SCV002460033 likely benign Li-Fraumeni syndrome 2021-02-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000776561 SCV002582250 likely benign Hereditary cancer-predisposing syndrome 2022-06-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002290024 SCV002582911 likely benign Li-Fraumeni syndrome 1 2022-06-18 criteria provided, single submitter clinical testing

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