ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.525+17G>A

dbSNP: rs2150942159
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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 RCV002091851 SCV002436072 likely benign not provided 2021-12-15 criteria provided, single submitter clinical testing

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