ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.191+24T>C

gnomAD frequency: 0.03673  dbSNP: rs34875865
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248270 SCV000309791 benign not specified criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715790 SCV005305304 benign not provided criteria provided, single submitter not provided

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