ClinVar Miner

Submissions for variant NM_021102.4(SPINT2):c.106+107C>T

gnomAD frequency: 0.07474  dbSNP: rs112797649
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
GeneDx RCV001645655 SCV001858773 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001645655 SCV005308546 benign not provided criteria provided, single submitter not provided

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