ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.1379-173C>G

gnomAD frequency: 0.00322  dbSNP: rs547839307
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002244377 SCV002512964 likely benign not provided 2021-05-17 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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