ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.526-10T>C

dbSNP: rs199771569
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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 RCV000944541 SCV001090512 likely benign not provided 2024-09-30 criteria provided, single submitter clinical testing

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