ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.3142+7G>A

dbSNP: rs1159766861
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002126028 SCV002452826 likely benign not provided 2022-02-24 criteria provided, single submitter clinical testing

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