ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.513C>A (p.Val171=)

dbSNP: rs140211154
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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 RCV002131527 SCV002451699 likely benign not provided 2021-05-16 criteria provided, single submitter clinical testing

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