ClinVar Miner

Submissions for variant NM_004343.4(CALR):c.817-9C>T

gnomAD frequency: 0.00988  dbSNP: rs74815302
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000966065 SCV001113352 benign not provided 2018-07-10 criteria provided, single submitter clinical testing
GeneDx RCV000966065 SCV002575198 likely benign not provided 2021-02-18 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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