ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.686-15T>C

gnomAD frequency: 0.00001  dbSNP: rs753877022
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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 RCV002130062 SCV002414375 likely benign not provided 2024-12-29 criteria provided, single submitter clinical testing

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