ClinVar Miner

Submissions for variant NM_015693.4(INTU):c.1869A>G (p.Val623=)

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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 RCV003854421 SCV004659349 likely benign not provided 2023-04-13 criteria provided, single submitter clinical testing

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