ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.791+7G>C

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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 RCV003575866 SCV004370069 likely benign not provided 2023-05-12 criteria provided, single submitter clinical testing

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