ClinVar Miner

Submissions for variant NC_000007.14:g.156764209G>A

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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 RCV002735735 SCV003016299 benign Holoprosencephaly 3 2024-10-23 criteria provided, single submitter clinical testing

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