ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.1130-22A>G

gnomAD frequency: 0.32652  dbSNP: rs6789961
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 RCV000242731 SCV000309784 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001536767 SCV001753574 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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