ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.3496+174C>T

gnomAD frequency: 0.00653  dbSNP: rs72902629
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 RCV001558543 SCV001780514 likely benign not provided 2018-09-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001558543 SCV005257067 likely benign not provided criteria provided, single submitter not provided

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