ClinVar Miner

Submissions for variant NM_000546.6(TP53):c.-73C>A

dbSNP: rs886053514
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000276492 SCV000407076 uncertain significance Li-Fraumeni syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000308260 SCV000407077 uncertain significance Dyskeratosis Congenita, Recessive 2016-06-14 criteria provided, single submitter clinical testing

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