ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.1518-48C>T

gnomAD frequency: 0.05391  dbSNP: rs62487918
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 RCV000243003 SCV000310110 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001650854 SCV001867202 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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