ClinVar Miner

Submissions for variant NM_021076.4(NEFH):c.883+16G>A

gnomAD frequency: 0.00089  dbSNP: rs534281794
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001699718 SCV002489640 benign not provided 2025-01-26 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699718 SCV001923337 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699718 SCV001930188 likely benign not provided no assertion criteria provided clinical testing

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