ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.759G>A (p.Glu253=)

dbSNP: rs1342987313
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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 RCV002176916 SCV002337081 likely benign not provided 2022-01-27 criteria provided, single submitter clinical testing

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