ClinVar Miner

Submissions for variant NM_001386140.1(MTTP):c.2218-32T>G

gnomAD frequency: 0.07351  dbSNP: rs41275719
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 RCV001657404 SCV001870090 benign not provided 2018-09-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001657404 SCV005301455 benign not provided criteria provided, single submitter not provided

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