ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.573C>T (p.His191=)

dbSNP: rs2150941365
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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 RCV001441569 SCV001644500 likely benign not provided 2021-10-18 criteria provided, single submitter clinical testing

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