ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.5199+7C>T

dbSNP: rs2145399219
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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 RCV002100543 SCV002384730 likely benign not provided 2022-06-04 criteria provided, single submitter clinical testing

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