ClinVar Miner

Submissions for variant NM_002528.7(NTHL1):c.792-11del

dbSNP: rs2150938017
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002212289 SCV002351710 benign not provided 2023-11-05 criteria provided, single submitter clinical testing

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